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PMID: 6862433 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

High-resolution chromosome analysis of phenotypically abnormal patients with apparently balanced structural rearrangements.

Human genetics ·Vol. 63 ·No. 4 ·1983-00-00 ·Pages 310-4

Raimondi SC, Luthardt FW, Summitt RL, Martens PR

Abstract

Thirteen phenotypically abnormal patients with previously identified de novo or familial, apparently balanced, chromosome rearrangements were reexamined with high-resolution techniques. No definite imbalance could be demonstrated in any of the cases. However, some breakpoints were reassigned to more specific sub-bands and others to totally different bands. The study confirmed translocation reciprocity in some cases in which metaphase banding techniques failed to allow such determination. In one patient an apparent extra dark band was observed which could be explained by limited uncoiling, intraband exchange or small band duplication. In two patients limited uncoiling was observed in one derivative chromosome. Tissue-limited mosaicism was discovered in cultured fibroblasts from one of the seven patients evaluated.

MeSH Terms
Child Chromosome Aberrations/genetics Chromosome Banding Chromosome Disorders Cytogenetics Female Humans Intellectual Disability/genetics Karyotyping Male Mosaicism Phenotype Translocation, Genetic
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Raimondi S C
Luthardt F W
Summitt R L
Martens P R
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13 references, click to expand
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Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
Published
1983-00-00
Pages
310-4
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
Grants
PHS HHS · 900 · United States
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