Additional patients with 4q deletion: Severe growth delay and polycystic kidney disease associated with 4q21q22 loss
Author:
Affiliation:
1. Department of Pediatrics, Koshigaya Hospital; Dokkyo Medical University; Saitama Japan
2. Department of Genetic Counseling, Graduate School of Human Genetics and Science; Ochanomizu University; Tokyo Japan
Funder
Dokkyo Medical University, Investigator-Initiated Research
Publisher
Wiley
Subject
Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/ped.12742/fullpdf
Reference5 articles.
1. Partial monosomy of long arm of chromosome 4 due to interstitial deletion;McDermott;Hum. Genet.,1980
2. Deletions of different segments of the long arm of chromosome 4;Mitchell;Am. J. Med. Genet.,1981
3. A 4q21-q22 deletion in a girl with severe growth retardation;Harada;Clin. Genet.,2002
4. Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech;Bonnet;J. Med. Genet.,2010
5. Expanding the spectrum of microdeletion 4q21 syndrome: A partial phenotype with incomplete deletion of the minimal critical region and a new association with cleft palate and Pierre Robin sequence;Bhoj;Am. J. Med. Genet. A,2013
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