Unbalanced karyotype with normal phenotype in a family with translocation (8;13) (p21;q22)
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1985.tb00237.x/fullpdf
Reference21 articles.
1. Small structural changes of chromosome 8;Beighle;Hum. Genet.,1977
2. Délétion partielle du bras court de chromosome 8;Bresson;Ann. Génét.,1977
3. Partial deletion of the long arm of chromosome no. 13;Cushieri;Hum. Genet.,1977
4. Two cases of an abnormal short arm of chromosome 8(8p +) associated with mental retardation;Hongell;Clin Genet.,1978
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1. Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia;American Journal of Medical Genetics Part A;2009-07-15
2. Prenatal diagnosis ofde novo partial trisomy 13q (13q22 ? qter) and partial monosomy 8p (8p23.3 ? pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart;Prenatal Diagnosis;2005
3. A deletion map of the human Yq11 region: Implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis;Genomics;1991-10
4. Duplication of euchromatin without phenotypic effects: A variant of chromosome 16;American Journal of Medical Genetics;1990-05
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