Update more than 112 ring chromosome 13

Top images of ring chromosome 13 by website dienmayquynhon.com.vn compilation. JCM | Free Full-Text | Rare within Rare: A Girl with Severe Haemophilia A and Turner Syndrome. Chromosomal Abnormalities. As we all know there are 23 pairs of… | by Zaira Bhatti | Medium. A case of mosaic ring chromosome 13 syndrome. GTG-banded karyotype from cultured peripheral blood lymphocytes of the… | Download Scientific Diagram. Ring Chromosome 18 in a Patient with Multiple Anomalies*

Interstitial Duplication and Distal Deletion in a Ring Chromosome 13 with  Pulmonary Atresia and Ventricular Septal Defect: A Case Report and Review  of Literature | Semantic ScholarInterstitial Duplication and Distal Deletion in a Ring Chromosome 13 with Pulmonary Atresia and Ventricular Septal Defect: A Case Report and Review of Literature | Semantic Scholar – #1

A karyotype of 46,XY,r(13). The arrows indicate the breakpoints. r(13)... |  Download Scientific DiagramA karyotype of 46,XY,r(13). The arrows indicate the breakpoints. r(13)… | Download Scientific Diagram – #2

Duplication of chromosome segment 12q13-15 in a lipomatous tumor with  minimal nuclear atypia: A case reportDuplication of chromosome segment 12q13-15 in a lipomatous tumor with minimal nuclear atypia: A case report – #3

Figure 3 from Ring chromosome 13 in an infant with ambiguous genitalia. |  Semantic ScholarFigure 3 from Ring chromosome 13 in an infant with ambiguous genitalia. | Semantic Scholar – #4

Reevaluation of the origin of a marker chromosome in a patient with 47,XX,r( 13)(p11q34), +mar by molecular cytogeneticsReevaluation of the origin of a marker chromosome in a patient with 47,XX,r( 13)(p11q34), +mar by molecular cytogenetics – #5

Clinical and cytogenetic analysis of terminal 22q13.3 deletion in two  patients with ring chromosome 22 Ismail S, Kamel AK, Ashaat EA, Mohamed AM,  Zaki MS, Aboul-Ezz EH, Hammad SA, Sayed IS, ElClinical and cytogenetic analysis of terminal 22q13.3 deletion in two patients with ring chromosome 22 Ismail S, Kamel AK, Ashaat EA, Mohamed AM, Zaki MS, Aboul-Ezz EH, Hammad SA, Sayed IS, El – #6

Chromosomes and Chromosomal Abnormalities | Neupsy KeyChromosomes and Chromosomal Abnormalities | Neupsy Key – #7

Azoospermia and ring chromosome 9—a case report | Journal of Assisted  Reproduction and GeneticsAzoospermia and ring chromosome 9—a case report | Journal of Assisted Reproduction and Genetics – #8

Ring chromosome 13 syndromeRing chromosome 13 syndrome – #9

PDF] Ring Chromosome 13 in an Infant Girl | Semantic ScholarPDF] Ring Chromosome 13 in an Infant Girl | Semantic Scholar – #10

Ring chromosome 7: Report of the fifth caseRing chromosome 7: Report of the fifth case – #11

What Is Karyotyping? Methods and Their Significance | SynthegoWhat Is Karyotyping? Methods and Their Significance | Synthego – #12

Chromosomes in the genomic age. Preserving cytogenomic competence of  diagnostic genome laboratories. - Abstract - Europe PMCChromosomes in the genomic age. Preserving cytogenomic competence of diagnostic genome laboratories. – Abstract – Europe PMC – #13

Refined genotype–phenotype correlations in cases of chromosome 6p deletion  syndromes | European Journal of Human GeneticsRefined genotype–phenotype correlations in cases of chromosome 6p deletion syndromes | European Journal of Human Genetics – #14

PDF] A Case of Autism with Ring Chromosome 14 | Semantic ScholarPDF] A Case of Autism with Ring Chromosome 14 | Semantic Scholar – #15

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Towards New Approaches to Evaluate Dynamic Mosaicism in Ring Chromosome 13  Syndrome. - Document - Gale Academic OneFileTowards New Approaches to Evaluate Dynamic Mosaicism in Ring Chromosome 13 Syndrome. – Document – Gale Academic OneFile – #16

Ring chromosome - WikipediaRing chromosome – Wikipedia – #17

Ring Chromosome D (13)Ring Chromosome D (13) – #18

Related HealthJournals - Chromosome Disorders: What Happens When Cell  Division Goes Wrong - StoryMDRelated HealthJournals – Chromosome Disorders: What Happens When Cell Division Goes Wrong – StoryMD – #19

Chromosomal causes of infertility (Chapter 7) - Textbook of Human  Reproductive GeneticsChromosomal causes of infertility (Chapter 7) – Textbook of Human Reproductive Genetics – #20

Figure 2 from [A case of mosaic ring chromosome 4 with subtelomeric 4p  deletion]. | Semantic ScholarFigure 2 from [A case of mosaic ring chromosome 4 with subtelomeric 4p deletion]. | Semantic Scholar – #21

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Chromosomal Abnormalities. As we all know there are 23 pairs of… | by Zaira  Bhatti | MediumChromosomal Abnormalities. As we all know there are 23 pairs of… | by Zaira Bhatti | Medium – #22

Ring chromosome 15 (a) found in an infant with Ring chromosome 15 (a) found in an infant with ” ring syndrome “… | Download Scientific Diagram – #23

Ring Chromosome 13 Syndrome - DoveMedRing Chromosome 13 Syndrome – DoveMed – #24

Patients I-V, VII-IX and XI-XIV, who present ring chromosomes 3, 4, 10,...  | Download Scientific DiagramPatients I-V, VII-IX and XI-XIV, who present ring chromosomes 3, 4, 10,… | Download Scientific Diagram – #25

Nondisjunction and chromosomal anomaliesNondisjunction and chromosomal anomalies – #26

Ring20 Research & Support UK CIO - What exactly is a ring chromosome?  Chromosomes usually have a top and a bottom, but in a ring chromosome for  some reason a chromosome formsRing20 Research & Support UK CIO – What exactly is a ring chromosome? Chromosomes usually have a top and a bottom, but in a ring chromosome for some reason a chromosome forms – #27

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Decoding the Ring ChromosomeDecoding the Ring Chromosome – #28

Karyotype Explanation Tool - Ring20 Research and Support UK CIOKaryotype Explanation Tool – Ring20 Research and Support UK CIO – #29

A case of mosaic ring chromosome 13 syndromeA case of mosaic ring chromosome 13 syndrome – #30

What is a ring chromosome - Ring20 Research and Support UK CIOWhat is a ring chromosome – Ring20 Research and Support UK CIO – #31

Clinical, cytogenetic, and molecular findings in a patient with ring  chromosome 4: case report and literature review | BMC Medical Genomics |  Full TextClinical, cytogenetic, and molecular findings in a patient with ring chromosome 4: case report and literature review | BMC Medical Genomics | Full Text – #32

Ring Chromosome 20 – this is what you need to know | Beyond the Ion ChannelRing Chromosome 20 – this is what you need to know | Beyond the Ion Channel – #33

A case of ring chromosome 18 syndrome treated with a combined  orthodontic-prosthodontic approach. | Semantic ScholarA case of ring chromosome 18 syndrome treated with a combined orthodontic-prosthodontic approach. | Semantic Scholar – #34

Figure 1 from Severe anomalies associated with ring chromosome 7. |  Semantic ScholarFigure 1 from Severe anomalies associated with ring chromosome 7. | Semantic Scholar – #35

The ring 14 syndrome - ScienceDirectThe ring 14 syndrome – ScienceDirect – #36

JCDD | Free Full-Text | A Review of Recent Developments in Turner Syndrome  ResearchJCDD | Free Full-Text | A Review of Recent Developments in Turner Syndrome Research – #37

Complex genetic aberrancies including JAK2 double minute by FISH. (A)... |  Download Scientific DiagramComplex genetic aberrancies including JAK2 double minute by FISH. (A)… | Download Scientific Diagram – #38

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Karyotype — Knowledge HubKaryotype — Knowledge Hub – #39

Human ring chromosome registry for cases in the Chinese population:  re-emphasizing Cytogenomic and clinical heterogeneity and reHuman ring chromosome registry for cases in the Chinese population: re-emphasizing Cytogenomic and clinical heterogeneity and re – #40

Characterization of a rare mosaic X-ring chromosome in a patient with  Turner syndrome | Molecular Cytogenetics | Full TextCharacterization of a rare mosaic X-ring chromosome in a patient with Turner syndrome | Molecular Cytogenetics | Full Text – #41

Genes | Free Full-Text | Clinical and Genetic Aspects of  Phelan–McDermid Syndrome: An Interdisciplinary Approach to ManagementGenes | Free Full-Text | Clinical and Genetic Aspects of Phelan–McDermid Syndrome: An Interdisciplinary Approach to Management – #42

Educational Case: Cytogenetics - ScienceDirectEducational Case: Cytogenetics – ScienceDirect – #43

PDF) Towards New Approaches to Evaluate Dynamic Mosaicism in Ring  Chromosome 13 SyndromePDF) Towards New Approaches to Evaluate Dynamic Mosaicism in Ring Chromosome 13 Syndrome – #44

PDF] Smallest critical region for microcephaly in a patient with mosaic ring  chromosome 13. | Semantic ScholarPDF] Smallest critical region for microcephaly in a patient with mosaic ring chromosome 13. | Semantic Scholar – #45

PDF) Ring chromosome 13 syndrome characterized by high resolution array  based comparative genomic hybridization in patient with 47, XYY syndrome: A  case reportPDF) Ring chromosome 13 syndrome characterized by high resolution array based comparative genomic hybridization in patient with 47, XYY syndrome: A case report – #46

PDF) Case Report of Ring Chromosome 13: 46,XX,r(13)(p13q34)/46,XX,dic r(13; 13)(p13q34;p13q34)PDF) Case Report of Ring Chromosome 13: 46,XX,r(13)(p13q34)/46,XX,dic r(13; 13)(p13q34;p13q34) – #47

Plantae | A Novel Role of Ring Chromosomes as Evolutionary Drivers of  Herbicide Resistance | PlantaePlantae | A Novel Role of Ring Chromosomes as Evolutionary Drivers of Herbicide Resistance | Plantae – #48

Turner syndrome - WikipediaTurner syndrome – Wikipedia – #49

Chromosomes in the genomic age. Preserving cytogenomic competence of  diagnostic genome laboratories | European Journal of Human GeneticsChromosomes in the genomic age. Preserving cytogenomic competence of diagnostic genome laboratories | European Journal of Human Genetics – #50

The patient's karyogram demonstrates a ring chromosome 18. | Download  Scientific DiagramThe patient’s karyogram demonstrates a ring chromosome 18. | Download Scientific Diagram – #51

Compound phenotype in a girl with r(22), concomitant microdeletion  22q13.32-q13.33 and mosaic monosomy 22 | Molecular Cytogenetics | Full TextCompound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22 | Molecular Cytogenetics | Full Text – #52

Children | Free Full-Text | Wolf-Hirschhorn Syndrome: Clinical and Genetic  Study of 7 New Cases, and Mini ReviewChildren | Free Full-Text | Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini Review – #53

Karyotypes demonstrated in cells exposed to 5 Gy of radiation. Arrows... |  Download Scientific DiagramKaryotypes demonstrated in cells exposed to 5 Gy of radiation. Arrows… | Download Scientific Diagram – #54

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PDF) Molecular cytogenetic and phenotypic characterization of ring  chromosome 13 in three unrelated patientsPDF) Molecular cytogenetic and phenotypic characterization of ring chromosome 13 in three unrelated patients – #55

PDF) Ring Chromosome 13 and Ambiguous Genitalia | Gül Mutlu - Academia.eduPDF) Ring Chromosome 13 and Ambiguous Genitalia | Gül Mutlu – Academia.edu – #56

Meiotic and mitotic behaviour of a ring/deleted chromosome 22 in human  embryos determined by preimplantation genetic diagnosis for a maternal  carrier | Molecular Cytogenetics | Full TextMeiotic and mitotic behaviour of a ring/deleted chromosome 22 in human embryos determined by preimplantation genetic diagnosis for a maternal carrier | Molecular Cytogenetics | Full Text – #57

GTG-banded karyotype from cultured peripheral blood lymphocytes of the... |  Download Scientific DiagramGTG-banded karyotype from cultured peripheral blood lymphocytes of the… | Download Scientific Diagram – #58

PDF] Ring chromosome 13 in an infant with ambiguous genitalia. | Semantic  ScholarPDF] Ring chromosome 13 in an infant with ambiguous genitalia. | Semantic Scholar – #59

PDF] Mosaic Ring Chromosome 6 in an Infant with Significant Patent Ductus  Arteriosus and Multiple Congenital Anomalies | Semantic ScholarPDF] Mosaic Ring Chromosome 6 in an Infant with Significant Patent Ductus Arteriosus and Multiple Congenital Anomalies | Semantic Scholar – #60

Chromosomal Micro Array - Ring20 Research and Support UK CIOChromosomal Micro Array – Ring20 Research and Support UK CIO – #61

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PDF) Ring Chromosome 13 and Ambiguous GenitaliaPDF) Ring Chromosome 13 and Ambiguous Genitalia – #62

A Comprehensive and Clinical Review of Chromosome 9 Ring SyndromeA Comprehensive and Clinical Review of Chromosome 9 Ring Syndrome – #63

Small supernumerary marker chromosome - WikipediaSmall supernumerary marker chromosome – Wikipedia – #64

Chromosomal Aberrations and Down syndromeChromosomal Aberrations and Down syndrome – #65

Cytology. Cytology. seem to account very well for the range of chromosome  numbers in Crepis (Babcock, 1947) especially since interspecific hybrids  between species with n = 4 and n = 3Cytology. Cytology. seem to account very well for the range of chromosome numbers in Crepis (Babcock, 1947) especially since interspecific hybrids between species with n = 4 and n = 3 – #66

Ring chromosome 20 syndromeRing chromosome 20 syndrome – #67

PDF] The ring 14 syndrome. | Semantic ScholarPDF] The ring 14 syndrome. | Semantic Scholar – #68

Ring 13 FTNW - Unique - The Rare Chromosome Disorder Support ...Ring 13 FTNW – Unique – The Rare Chromosome Disorder Support … – #69

Neocentromere - WikipediaNeocentromere – Wikipedia – #70

Creating a functional single-chromosome yeast | NatureCreating a functional single-chromosome yeast | Nature – #71

Genetic ClinicsGenetic Clinics – #72

Ring Chromosomes - StoryMDRing Chromosomes – StoryMD – #73

Boy with celiac disease, malformations, and ring chromosome 13 with  deletion 13q32⃙qterBoy with celiac disease, malformations, and ring chromosome 13 with deletion 13q32⃙qter – #74

e (A) Karyotype of child showing Trisomy 21. (B) Karyotype of child... |  Download Scientific Diagrame (A) Karyotype of child showing Trisomy 21. (B) Karyotype of child… | Download Scientific Diagram – #75

The Chromosome 18 Conditions - YouTubeThe Chromosome 18 Conditions – YouTube – #76

Ring Chromosomes | SpringerLinkRing Chromosomes | SpringerLink – #77

Frontal view of chromosomes from a. Patient I-ring 4; b. Patient... |  Download Scientific DiagramFrontal view of chromosomes from a. Patient I-ring 4; b. Patient… | Download Scientific Diagram – #78

Ring 22 FTNWRing 22 FTNW – #79

Molecular and cytogenetic characterisation of an unusual case of partial  trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13 ;13)(q10;q14) | Journal of Medical GeneticsMolecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13 ;13)(q10;q14) | Journal of Medical Genetics – #80

Mechanisms of ring chromosome formation, ring instability and clinical  consequences | BMC Medical Genetics | Full TextMechanisms of ring chromosome formation, ring instability and clinical consequences | BMC Medical Genetics | Full Text – #81

Two Cases with Ring Chromosome 13 at either End of the Phenotypic Spectrum  | Request PDFTwo Cases with Ring Chromosome 13 at either End of the Phenotypic Spectrum | Request PDF – #82

The Association of Ring Chromosome 13 and Duodenal ObstructionThe Association of Ring Chromosome 13 and Duodenal Obstruction – #83

PDF] Thai girl with ring chromosome 18 (46XX, r18). | Semantic ScholarPDF] Thai girl with ring chromosome 18 (46XX, r18). | Semantic Scholar – #84

PDF] Ring Chromosome and Clinical Findings: Reports Cases of 4 Different  Chromosomes in Beninese Population | Semantic ScholarPDF] Ring Chromosome and Clinical Findings: Reports Cases of 4 Different Chromosomes in Beninese Population | Semantic Scholar – #85

Ring chromosome formation and dynamic mosaicism by... | Download Scientific  DiagramRing chromosome formation and dynamic mosaicism by… | Download Scientific Diagram – #86

Chromosomal Abnormalities - ppt downloadChromosomal Abnormalities – ppt download – #87

Autosomal Ring Chromosomes - Chromosome Abnormalities and Genetic  Counseling , 3rd EditionAutosomal Ring Chromosomes – Chromosome Abnormalities and Genetic Counseling , 3rd Edition – #88

Figure 2 from Ring chromosome 11 with KMT2A (MLL; 11q23) amplification and  deletion in a patient with acute myeloid leukemia | Semantic ScholarFigure 2 from Ring chromosome 11 with KMT2A (MLL; 11q23) amplification and deletion in a patient with acute myeloid leukemia | Semantic Scholar – #89

SciELO - Brasil - Epilepsy and ring chromosome 20: case report Epilepsy and ring  chromosome 20: case reportSciELO – Brasil – Epilepsy and ring chromosome 20: case report Epilepsy and ring chromosome 20: case report – #90

Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal  samples: chromosomal distribution, clinical findings, and UPD studies |  European Journal of Human GeneticsForty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies | European Journal of Human Genetics – #91

Case Report Towards New Approaches to Evaluate Dynamic Mosaicism in Ring  Chromosome 13 SyndromeCase Report Towards New Approaches to Evaluate Dynamic Mosaicism in Ring Chromosome 13 Syndrome – #92

PDF) A Case with a Ring Chromosome 13 in a Cohort of 203 Children with  Non-Syndromic Autism and Review of the Cytogenetic LiteraturePDF) A Case with a Ring Chromosome 13 in a Cohort of 203 Children with Non-Syndromic Autism and Review of the Cytogenetic Literature – #93

Trisomy 13: MedlinePlus GeneticsTrisomy 13: MedlinePlus Genetics – #94

JCM | Free Full-Text | Rare within Rare: A Girl with Severe Haemophilia A  and Turner SyndromeJCM | Free Full-Text | Rare within Rare: A Girl with Severe Haemophilia A and Turner Syndrome – #95

Trisomy 13- Patau syndrome Mental deficiency; Severe central nervous system  malformations; Severe central nervous system malformations; - ppt downloadTrisomy 13- Patau syndrome Mental deficiency; Severe central nervous system malformations; Severe central nervous system malformations; – ppt download – #96

13q deletion syndrome - Wikipedia13q deletion syndrome – Wikipedia – #97

Two Siblings With Similar Phenotypes: One of Them Had Ring 20 Chromosome -  F. Irsel Tezer, Dilek Aktas, Mehmet Alikasifoglu, Serap Saygi, 2013Two Siblings With Similar Phenotypes: One of Them Had Ring 20 Chromosome – F. Irsel Tezer, Dilek Aktas, Mehmet Alikasifoglu, Serap Saygi, 2013 – #98

PDF] Ring Chromosome 4 in a Child with Multiple Congenital Abnormalities: A  Case Report and Review of the Literature | Semantic ScholarPDF] Ring Chromosome 4 in a Child with Multiple Congenital Abnormalities: A Case Report and Review of the Literature | Semantic Scholar – #99

Genes | Free Full-Text | 46,XY,r(8)/45,XY,−8 Mosaicism as a Possible  Mechanism of the Imprinted Birk-Barel Syndrome: A Case StudyGenes | Free Full-Text | 46,XY,r(8)/45,XY,−8 Mosaicism as a Possible Mechanism of the Imprinted Birk-Barel Syndrome: A Case Study – #100

Ring Chromosome 18 in a Patient with Multiple Anomalies*Ring Chromosome 18 in a Patient with Multiple Anomalies* – #101

Children | Free Full-Text | 18p Deletion Syndrome Originating from Rare  Unbalanced Whole-Arm Translocation between Chromosomes 13 and 18: A Case  Report and Literature ReviewChildren | Free Full-Text | 18p Deletion Syndrome Originating from Rare Unbalanced Whole-Arm Translocation between Chromosomes 13 and 18: A Case Report and Literature Review – #102

Figure 2 from Ring chromosome 14 syndrome presenting with intractable  epilepsy: a case report. | Semantic ScholarFigure 2 from Ring chromosome 14 syndrome presenting with intractable epilepsy: a case report. | Semantic Scholar – #103

Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult  patient with multiple congenital anomalies | Molecular Cytogenetics | Full  TextLow grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomalies | Molecular Cytogenetics | Full Text – #104

Diagnostics | Free Full-Text | Prenatal Sonographic Features of Ring  Chromosome 15: A Case Report and Literature ReviewDiagnostics | Free Full-Text | Prenatal Sonographic Features of Ring Chromosome 15: A Case Report and Literature Review – #105

Mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome  21: Prenatal diagnosis, molecular cytogenetic characterization, and  association with 2-Mb deletion of 21q21.1–q21.2 and 5-Mb deletion of  21q22.3 - ScienceDirectMosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: Prenatal diagnosis, molecular cytogenetic characterization, and association with 2-Mb deletion of 21q21.1–q21.2 and 5-Mb deletion of 21q22.3 – ScienceDirect – #106

Figure 3 from Complex karyotype including ring chromosome 11 in a patient  with acute myeloid leukemia: case report | Semantic ScholarFigure 3 from Complex karyotype including ring chromosome 11 in a patient with acute myeloid leukemia: case report | Semantic Scholar – #107

Ring chromosome 15 – cytogenetics and mapping arrays: a case report and  review of the literature | Journal of Medical Case Reports | Full TextRing chromosome 15 – cytogenetics and mapping arrays: a case report and review of the literature | Journal of Medical Case Reports | Full Text – #108

Partial karyotype showing ring chromosome 15, i.e. r(15)(p11.2q26) |  Download Scientific DiagramPartial karyotype showing ring chromosome 15, i.e. r(15)(p11.2q26) | Download Scientific Diagram – #109

Ring chromosome 13 and ambiguous genitalia. - Abstract - Europe PMCRing chromosome 13 and ambiguous genitalia. – Abstract – Europe PMC – #110

PDF] Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and  disomy 18: perinatal findings and molecular cytogenetic characterization by  fluorescence in situ hybridization and array comparative genomic  hybridization. | Semantic ScholarPDF] Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization. | Semantic Scholar – #111

Clinical, cytogenetic and molecular analyses of a rare case with ring  chromosome 15 and review of the literature - ScienceDirectClinical, cytogenetic and molecular analyses of a rare case with ring chromosome 15 and review of the literature – ScienceDirect – #112

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