Meiotic consequences of an intrachromosomal insertion of chromosome No. 1: a family pedigree-Reference-Cited by-同舟云学术

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Meiotic consequences of an intrachromosomal insertion of chromosome No. 1: a family pedigree

Published:2008-04-23 Issue:5 Volume:12 Page:303-313
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Pan S. F.,Fatora S. R.,Sorg R.,Garver K. L.,Steele M. W.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1977.tb00945.x/fullpdf

Reference12 articles.

1. “Cri du chat” syndrome with maternal insertional translocation;Berger;Chin. Genet.,1974

2. Familial mental retardation in a family with an inherited chromosome rearrangement;Chundley;J. med. Cruet.,1974

3. Complex five-break rearrangement;Fitzgerald;Chin. Genet.,1974

4. Familial insertional translocation;Grace;Lancet,1972

5. An interstitial trans-location: chromosome No. 1p to 4q;Gray;Lancet,1972

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1. A pure familial 6q15q21 split duplication associated with obesity and transmitted with partial reduction;American Journal of Medical Genetics Part A;2015-04-21

2. PGD for a carrier of an intrachromosomal insertion using aCGH;Systems Biology in Reproductive Medicine;2014-09-23

3. De novo Deletion of 1q31.1q32.1 in a Patient with Developmental Delay and Behavioral Disorders;Cytogenetic and Genome Research;2012

4. Molecular characterization of a patient with an interstitial 1q deletion [del(1)(q24.1q25.3)] and distinctive skeletal abnormalities;American Journal of Medical Genetics Part A;2008-11-15

5. INTRACHROMOSOMAL INSERTION OF CHROMOSOME 13 IN A FAMILY WITH PSYCHOSIS AND MENTAL SUBNORMALITY;Journal of Intellectual Disability Research;2008-06-28

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