 |
|
2q37 Deletion syndrome confirmed by high-resolution cytogenetic analysis
Eun-Kyung Cho, Jinsup Kim, Aram Yang, Sung Yoon Cho, Dong-Kyu Jin
Ann Pediatr Endocrinol Metab. 2017;22(2):129-132. Published online 2017 Jun 28 DOI: https://doi.org/10.6065/apem.2017.22.2.129
|
|
Citations to this article as recorded by
 A Cytogenetic Study of Turkish Children with Global Developmental Delay
Osman Demirhan, Özlem Hergüner, Erdal Tunç
Journal of Pediatric Genetics.2022;[Epub] CrossRef Genotype and phenotype correlation in 103 individuals with 2q37 deletion syndrome reveals incomplete penetrance and supports HDAC4 as the primary genetic contributor
Trang N. Le, Stephen R. Williams, Joseph T. Alaimo, Sarah H. Elsea
American Journal of Medical Genetics Part A.2019;[Epub] CrossRef Brachydactyly mental retardation syndrome with growth hormone deficiency
Alireza Arefzadeh, Pooyan Khalighinejad, Bahar Ataeinia, Pegah Parvar
Endocrinology, Diabetes & Metabolism Case Reports.2018;[Epub] CrossRef
|