Chimerism for 20q11.2 microdeletion of GDF5 explains discordant phenotypes in monochorionic-diamniotic twins-Reference-Cited by-同舟云学术

Chimerism for 20q11.2 microdeletion of GDF5 explains discordant phenotypes in monochorionic-diamniotic twins

Published:2017-09-08 Issue:12 Volume:173 Page:3182-3188
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Meredith Matthew M.¹^ORCID,Crabb Beau²,Vargas Marcelo²,Hirsch Betsy A.¹

Affiliation:

1. Division of Molecular Pathology and Genomics; Department of Laboratory Medicine and Pathology; University of Minnesota Medical School; Minneapolis Minnesota

2. Department of Medical Genetics and Genomics; Children's Minnesota; Minneapolis Minnesota

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference23 articles.

1. Two novel homozygous missense mutations in the GDF5 gene cause brachydactyly type C;Al-Qattan;American Journal Of Medical Genetics, Part A,2015

2. Clonal origins of ETV6-RUNX1+ acute lymphoblastic leukemia: Studies in monozygotic twins;Alpar;Leukemia,2015

3. Major feeding difficulties in the first reported case of interstitial 20q11.22-q12 microdeletion and molecular cytogenetic characterization;Callier;American Journal of Medical Genetics Part A,2006

4. Chimerism in monochorionic dizygotic twins: Case study and review;Chen;American Journal of Medical Genetics Part A,2013

5. Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1;Crow,;American Journal of Medical Genetics Part A,2015

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1. Monozygotic twins discordant for homologous Robertsonian translocation trisomy 21 of 46, XX, + 21, der (21;21) (q10; q10) in a twin-to-twin transfusion syndrome, case report;BMC Pregnancy and Childbirth;2021-01-30

2. First Report of Low-Rate Mosaicism for 20q11.21q12 Deletion and Delineation of the Associated Disorder;Cytogenetic and Genome Research;2018