Document Detail


Duplication 11p11.3 leads to 14.1 to meiotic crossing--over.
MedLine Citation:
PMID:  7211949     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
An infant with macular dysfunction, cleft lip and palate, and developmental delay was shown to have an inverted duplication of 11p11.3 leads to p14.1 on the basis of meiotic recombination subsequent to an intrachromosomal "shift" in his mother. A half-sister had previously been shown [3] to have the reciprocal recombinant with resultant deletion of 11p11.3 leads to 11p14.1.
Authors:
R J Strobel; V M Riccardi; D H Ledbetter; H M Hittner
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Publication Detail:
Type:  Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  American journal of medical genetics     Volume:  7     ISSN:  0148-7299     ISO Abbreviation:  Am. J. Med. Genet.     Publication Date:  1980  
Date Detail:
Created Date:  1981-05-28     Completed Date:  1981-05-28     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  7708900     Medline TA:  Am J Med Genet     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  15-20     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Abnormalities, Multiple / genetics
Chromosome Aberrations / genetics*
Chromosome Disorders
Chromosomes, Human, 6-12 and X*
Cleft Lip / genetics
Cleft Palate / genetics
Crossing Over, Genetic*
DNA Replication*
Dermatoglyphics
Humans
Infant, Newborn
Karyotyping
Male
Meiosis*
Phenotype
Grant Support
ID/Acronym/Agency:
1 RO1 CA25597-1/CA/NCI NIH HHS

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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