Two cases of an abnormal short arm of chromosome 8 (8p+) associated with mental retardation-Reference-Cited by-同舟云学术

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Two cases of an abnormal short arm of chromosome 8 (8p+) associated with mental retardation

Published:2008-04-23 Issue:2 Volume:13 Page:237-240
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Hongell Karin,Knuutila Sakari,Westermarck Thomas

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1978.tb04256.x/fullpdf

Reference6 articles.

1. Two cases of 8p trisomy in one sibship;Chiyo;Clin. Genet.,1975

2. Gene dose effect: regional mapping of human glutathione reductase on chromosome 8;George;Cytogenet. Cell Genet.,1976

3. Chromosome 8: trisomie complete et trisomie segmentates;Rethoré;Ann. Génét.,1977

4. Trisomy of the short arm of chromosome 8: Association with translocation between chromosomes 8 and 22 46, XY, 22-, t(8p22q) +;Rosenthal;Clin. Genet.,1973

5. Duplication-deficiency of the short arm of chromosome 8 following artificial insemination;Weleber;Ann. Génét.,1976

Cited by 23 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Dextrocardia, atrial septal defect, severe developmental delay, facial anomalies, and supernumerary ribs in a child with a complex unbalanced 8;22 translocation including partial 8p duplication;American Journal of Medical Genetics Part A;2012-02-02

2. A chromosome survey of 1062 mentally retarded patients. Evaluation of a long-term study at the Rinnekoti Institution, Finland;Hereditas;2009-02-12

3. Inv dup (8) (p21.1 → 22.1): further case report and a new hypothesis on the origin of the chromosome abnormality;Clinical Genetics;2008-06-28

4. Congenital cardiovascular malformations (CCVM) and structural chromosome abnormalities: a report of 9 cases and literature review;Clinical Genetics;2008-06-28

5. Familial Wolf's syndrome with a hidden 4p deletion by translocation of an 8p segment. Unbalanced inheritance from a maternal translocation (4;8)(p15.3;p22). Case report, review and risk estimates;Clinical Genetics;2008-04-23

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