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Split foot and developmental retardation associated with a deletion of three microsatellite markers in 7q21.2-q22.1

Split foot and developmental retardation associated with a deletion of three microsatellite... A deletion of 7q21.2-q22.1 has been found in a patient with split foot and developmental retardation. Molecular analysis using polymerase chain reaction (PCR) showed deletion of three microsatellite markers, D7S527, D7S479 and D7S554, in the patient's paternal chromosome. These results pinpoint the critical region for an ectrodactyly locus (SHFD1) on chromosome 7. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Clinical Genetics Wiley

Split foot and developmental retardation associated with a deletion of three microsatellite markers in 7q21.2-q22.1

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References (30)

Publisher
Wiley
Copyright
1995 Blackwell Munksgaard
ISSN
0009-9163
eISSN
1399-0004
DOI
10.1111/j.1399-0004.1995.tb03930.x
Publisher site
See Article on Publisher Site

Abstract

A deletion of 7q21.2-q22.1 has been found in a patient with split foot and developmental retardation. Molecular analysis using polymerase chain reaction (PCR) showed deletion of three microsatellite markers, D7S527, D7S479 and D7S554, in the patient's paternal chromosome. These results pinpoint the critical region for an ectrodactyly locus (SHFD1) on chromosome 7.

Journal

Clinical GeneticsWiley

Published: Feb 1, 1995

Keywords: deletion 7q21.2-q22.1; evelopmental retardation; ectrodactyly; SHFD1; split foot

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