Interstitial deletion of the short arm of chromosome 7 without craniosynostosis-Reference-Cited by-同舟云学术

Interstitial deletion of the short arm of chromosome 7 without craniosynostosis

Published:2008-04-23 Issue:6 Volume:19 Page:456-461
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Bianchi Diana W.,Cirillo-Silengo Margherita,Luzzatti Luigi,Greenstein Robert M.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1981.tb02064.x/fullpdf

Reference7 articles.

1. Assignment of the structural gene for human β-glucuronidase to chromosome 7 and tetrameric association of sub-units in the enzyme molecule;Chern;Amer. J. hum. Genet.,1976

2. The human gene for β-glucuronidase is on chromosome 7;Francke;Amer. J. hum. Genet.,1976

3. A girl with karyotype 46, XX, del(7) (q ter-p15);Friedrich;Hum. Genet.,1975

4. Chromosome 7 short arm deletion and craniosynostosis. A 7p- syndrome;McPherson;Hum. Genet.,1976

5. Chromosome 7 short arm interstitial deletion (p14);Moedjono;Hum. Genet.,1978

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1. Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality;Clinical Genetics;2008-06-28

2. Deletions of the short arm of chromosome 7 without craniosynostosis;Clinical Genetics;2008-04-23

3. Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations;The American Journal of Human Genetics;2005-04

4. Novel X-chromosomal defect associated with abnormal ovarian function;Journal of Obstetrics and Gynaecology Research;2005-02

5. Facial dysgenesis: A novel facial syndrome with chromosome 7 deletion p15.1-21.1;American Journal of Medical Genetics;2003-01-24