16q21 is critical for 16q deletion syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1988.tb03464.x/fullpdf
Reference11 articles.
1. Fragile site on chromosome 16 and the 16q-syndrome;Brenholz;Am. J. Hum. Genet.,1982
2. Confirmation of a suspected 16q deletion in a dysmorphic child by flow karyotype analysis;Cooke;J. Med. Genet.,1987
3. Fryns syndrome without deletion 16q;Coté;Ann. Génét.,1980
4. Identical twins with deletion 16q syndrome: evidence that 16q12.2-q13 is the critical band region;Elder;Hum. Genet.,1984
5. Partial monosomy of the long arm of chromosome 16 in a malformed newborn: karyotype 46, XX, del(16) (q21);Fryns;Hum. Genet.,1977
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