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PMID: 511172 Published · ppublish English Case Reports Journal Article Research Support, U.S. Gov't, P.H.S.

Interstitial deletion of chromosome 13 and associated congenital anomalies.

Human genetics ·Vol. 52 ·No. 2 ·1979-11-00 ·Pages 169-73

Nichols WW, Miller RC, Hoffman E, Albert D, Weichselbaum RR, Nove J, Little JB

Abstract

An interstitial deletion of chromosome 13 with breakpoints at 13q22 and 13q32 is presented. The clinical findings associated with this deletion are discussed in relation to the correlations of specific chromosomal bands with constellations of congenital defects as described by Niebuhr and Ottosen (1973), Niebuhr (1977). Lewandowski and Yunis (1975), and Noel et al. (1976).

MeSH Terms
Abnormalities, Multiple/genetics Adult Chromosome Aberrations/genetics Chromosome Banding Chromosome Deletion Chromosome Disorders Chromosomes, Human, 13-15 Female Humans Karyotyping
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Nichols W W
Miller R C
Hoffman E
Albert D
Weichselbaum R R
Nove J
Little J B
References (24)
24 references, click to expand
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Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
DOI
10.1007/BF00271569
Published
1979-11-00
Pages
169-73
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
External Links
PubMed source DOI: 10.1007/BF00271569 View journal details
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