Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21 → q25) and del(1)(q41 → q43)
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1985.tb00242.x/fullpdf
Reference13 articles.
1. Terminal deletion of (1)(q42) and its phenotypical manifestations;Andrle;Hum. Genet.,1978
2. Terminal long-arm deletion of chromosome 1 in a male infant;Dignan;Hum. Genet.,1979
3. Interstitial deletion in the long arms of chromosome 1: 46, XY, del(l)(pter → q22::q25 → qter);Pablo;J. Med. Genet.,1980
4. Terminal deletion of the long arm of chromosome 1 in a malformed newborn;Kessel;Hum. Genet.,1978
5. Interstitial deletion 46, XY, del(1)(q2325);Martin;Hum. Genet.,1982
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3. Refinement of genotype-phenotype correlation in 18 patients carrying a 1q24q25 deletion;American Journal of Medical Genetics Part A;2015-02-25
4. Maternal intrachromosomal insertional translocation leads to recurrent 1q21.3q23.3 deletion in two siblings;American Journal of Medical Genetics Part A;2012-08-17
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