Trisomy 4p in four relatives: variability and lack of distinctive features in phenotypic expression
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1983.tb00087.x/fullpdf
Reference12 articles.
1. Two case of trisomy 4p with translocation t(4p -, 7q+) in several members of one family;Andrle;Hum. Genet.,1976
2. Brief clinical report: dup (4p15→4pter) in a 19-year-old woman resulting from a maternal 4; 14 translocation;Clark;Am. J. Med. Genet.,1982
3. 4p trisomy syndrome: report of 4 additional cases and segregation analysis of 21 families with different translocations;Crane;Am. J. Med. Genet.,1979
4. Trisomy 4p: five new observations and overview;Dallapiccola;Clin. Genet.,1977
5. Osservazione familiare di due casi di trisomia 4p;Dede;Minerva Pediatr.,1979
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2. A family with partial duplication/deletion 4p due to a balanced t (4; 15) (p16.2; p11.2) translocation;American Journal of Medical Genetics Part A;2011-02-23
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4. C;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007
5. Prenatal diagnosis of trisomy 4p: a new locus for holoprosencephaly?;Prenatal Diagnosis;2005
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