Deletions of the short arm of chromosome 7 without craniosynostosis
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1982.tb01382.x/fullpdf
Reference11 articles.
1. Interstitial deletion of the short arm of chromosome 7 without craniosynos-tosis;Bianchi;Clin. Genet.,1981
2. Partial monosomy 7 with interstitial deletion in two infants with differing congenital abnormalities;Crawfurd;J. med. Genet.,1979
3. Terminal 7p deletion and 1;7 translocation associated with craniosynostosis;Dhadial;Hum. Genet.,1979
4. A girl with karyotype 46, XX, del(7) (qter-p15:);Friedrich;Hum. Genet.,1975
5. An International System for Human Cytogenetic Nomenclature - High-Resolution Banding (1981);ISCN;Birth Defects: Original Article Series,1981
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1. Small 7p22.3 microdeletion: Case report of Snx8 haploinsufficiency and neurological findings;European Journal of Medical Genetics;2020-04
2. Cardiac malformation of partial trisomy 7p/monosomy 18p and partial trisomy 18p/monosomy 7p in siblings as a result of reciprocal unbalanced malsegregation—and review of the literature;European Journal of Pediatrics;2012-02-01
3. Delineation of a less than 200 kb minimal deleted region for cardiac malformations on chromosome 7p22;American Journal of Medical Genetics Part A;2011-06-10
4. Saethre-Chotzen syndrome with familial translocation at chromosome 7p22;American Journal of Medical Genetics;1993-10-01
5. Duplication 7p in a family with t(7;11): Association with anomalies of the anterior cranial base;American Journal of Medical Genetics;1987-07
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