Recombination aneusomy of chromosome 5 associated with multiple severe congenital malformations

Author:

Schroeder H. W.,Forbes S.,Mack L.,Davis S.,Norwood T. H.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference31 articles.

1. Partial monosomy 22 pter→qll in a newborn with the clinical features of trisomy 13 syndrome;Back;Ann. Genet.,1980

2. Familial partial monosomy 5p and trisomy 5q; three cases due to paternal pericentric inversion 5(p151q33);Beemer;Clin. Genet.,1984

3. Recurrence of holoprosencephaly in families with a positive history;Benke;Clin. Genet.,1983

4. Chromosome mosaicism associated with a case of cyclopia;Cohen;J. Pediatr.,1966

5. An update on the holoprosencephalic disorders;Cohen;J. Pediatr.,1982

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1. Chromosome Aberrations and Gene Mutations in Patients With Esophageal Atresia;Journal of Pediatric Gastroenterology & Nutrition;2013-12

2. Clinical and molecular cytogenetic studies in ring chromosome 5: Report of a child with congenital abnormalities;European Journal of Medical Genetics;2012-02

3. Holoprosencephaly: An update on cytogenetic abnormalities;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2010-02-15

4. Craniosynostosis in a patient with 2q37.3 deletion 5q34 duplication: Association of extra copy ofMSX2with craniosynostosis;American Journal of Medical Genetics Part A;2009-07

5. Genetic testing in other GI diseases;Best Practice & Research Clinical Gastroenterology;2009-04

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