Nine year old boy with chromosome 1q23.3-q25.1 deletion
Author:
Affiliation:
1. Department of Pediatrics; University of Nevada School of Medicine; Las Vegas Nevada
2. Genetics Division; Department of Pediatrics; University of Nevada School of Medicine; Las Vegas Nevada
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference14 articles.
1. Distinctive phenotype in 9 patients with deletion of chromosome 1q24q25;Burkardt;Am J Med Genet Part A,2011
2. Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip-palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12)(q24;q24);Callier;Eur J Med Genet,2007
3. Refinement of genotype-phenotype correlation in 18 patients carrying a 1q24q25 deletion;Chatron;Am J Med Genet Part A,2015
4. A case of autism with an interstitial 1q deletion (1q23. 3-24. 2) and a de novo translocation of chromosome 1q and 5q;Della Monica;Am J Med Genet Part A,2007
5. Interstitial deletion in the long arms of chromosome 1:46,XY,del(1)(pter q22:q25 qter);DePablo;J Med Genet,1980
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