Interstitial deletion of chromosome 7: A case report and review of the literature
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1982.tb01442.x/fullpdf
Reference26 articles.
1. Délétion interstitielle du bras long d'un chromosome 7 chez une enfant IeprCchaune;Ayraud;Ann. Genet.,1976
2. Two different chromosome abnormalities resulting from a translocation carrier father;Bass;J. Pediut.,1973
3. Two unrelated children with distal long arm deletion of chromosome 7: clinical features, cytogenetic and gene-mapping studies;Bernstein;Clin. Genet.,1980
4. Balanced 1(8;9)(q12;q33)pat carrier with phenotypic abnormalities attributable to a de novo terminal deletion of the long aim of chromosome 7;Biederman;Hum. Genet.,1978
5. Partial monosomy 7 with interstitial deletions in two infants with differing congenital abnormalities;Crawfurd;J. med. Genet.,1979
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1. Interstitial deletion of 7q22.1q31.1 in a boy with structural brain abnormality, cardiac defect, developmental delay, and dysmorphic features;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2016-04-20
2. A novel interstitial microdeletion of 7q22.1-7q22.3 detected by array comparative genomic hybridization;American Journal of Medical Genetics Part A;2011-10-14
3. The interstitial deletion of bands q33-35 of long arm of chromosome 7: a review with a new case report;Clinical Genetics;2008-06-28
4. An interstitial deletion of chromosome 7 at band q21: A case report and review;American Journal of Medical Genetics Part A;2005-02-24
5. Prenatal Diagnosis of a Partial Monosomy 7q11→q31 in a Fetus with Split Foot;Fetal Diagnosis and Therapy;2005
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