Malformations in a child with dup (7 pter-p15.1) and del (7 q36-qter) as a result of familial pericentric inversion
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1991.tb03056.x/fullpdf
Reference29 articles.
1. Clinical, chromosomal and enzymatic studies in four cases of rearrangements of chromosome 7;Baeteman;Clin Genet.,1985
2. Two unrelated children with distal long arm deletion of chromosome 7: clinical features, cytogenetic and gene marker studies;Bernstein;Clin. Genet.,1980
3. Two children with partial trisomy for 7p;Berry;J. Med. Genet.,1979
4. Balanced t(8;9)(q12;q33) pat carrier with phenotypic abnormalities attributable to a de novo terminal deletion of the long arm of chromosome 7;Biederman;Hum. Genet.,1978
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1. Discordant phenotypes in a mother and daughter with mosaic supernumerary ring chromosome 19 explained by a de novo 7q36.2 deletion and 7p22.1 duplication;American Journal of Medical Genetics Part A;2011-03-17
2. De novo duplication of 7pter→p21.2 and deletion of 9pter→p23.5: clinical and cytogenetic diagnosis;Clinical Genetics;2008-06-28
3. Inheritance of pericentric inversion in chromosome 7 through the three progenies and a newborn with congenital hydronephrosis diagnosed prenatally by fetal urine sampling;Fertility and Sterility;2008-01
4. Trisomy 7p resulting from 7p15;9p24 translocation: Report of a new case and review of associated medical complications;American Journal of Medical Genetics;2000-04-10
5. Molecular cytogenetic analysis and clinical findings in a newborn with prenatally diagnosed rec(7)dup(7q)inv(7)(p22q31.3)pat;Prenatal Diagnosis;1999-12
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