Interstitial deletion in the long arm of chromosome no. 5

Author:

Harprecht-Beato W.,Kaiser P.,Steuber E.,Reinhard W.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference9 articles.

1. Interstitial deletion in the long arm of chromosome 5;Centerwall;Amer. J. hum. Genet.,1978

2. A child with interstitial deletion of chromosome no. 5;Felding;Hereditas,1980

3. Evidence for localization of the gene for hexosaminidase B to the cen - q13 region of human chromosome 5 using mouse x human hybrid cells;George;Cytogenet. Cell Genet.,1978

4. Palmer , C. G. S. Coburn E. Leikoff 1977 46, XY, del(5)(pter to q21::q23 toqter) Repository of Chromosomal Variants and Anomalies in Man

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1. Deletions and duplications of developmental pathway genes in 5q31 contribute to abnormal phenotypes;American Journal of Medical Genetics Part A;2011-07-08

2. Interstitial deletion 5q14.3q21.3 with MEF2C haploinsufficiency and mild phenotype: When more is less;American Journal of Medical Genetics Part A;2011-05-12

3. Severe mental retardation, seizures, and hypotonia due to deletions ofMEF2C;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2010

4. NR2F1 deletion in a patient with a de novo paracentric inversion, inv(5)(q15q33.2), and syndromic deafness;American Journal of Medical Genetics Part A;2009-04-07

5. Ring chromosome 5;Clinical Genetics;2008-06-28

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