Literature DB >> 7160103

Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome.

M G Butler, S G Kaler, P L Yu, F J Meaney.   

Abstract

Metacarpophalangeal pattern profile (MCPP) was determined on 16 Prader-Willi patients. Chromosome analysis of 14 patients showed an interstitial deletion of the long arm of chromosome 15 in seven subjects and normal chromosome results for the remaining individuals. Two separate and distinguishable hand profiles for each group based on the chromosome findings were identified. Correlation studies confirmed the homogeneity of the chromosome deletion group relative to the Prader-Willi individuals with normal chromosomes. Discriminant analysis of Prader-Willi versus normal individuals produces a function of three MCPP variables plus age which may provide a useful tool for diagnosis.

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Year:  1982        PMID: 7160103      PMCID: PMC6218245          DOI: 10.1111/j.1399-0004.1982.tb01846.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  13 in total

1.  Metacarpophalangeal pattern profile analysis in Noonan syndrome.

Authors:  M G Butler; R Kumar; M F Davis; D D Gale; G A Dahir; F J Meaney
Journal:  Am J Med Genet       Date:  2000-05-15

2.  The developing role of anthropologists in medical genetics: anthropometric assessment of the Prader-Labhart-Willi syndrome as an illustration.

Authors:  F J Meaney; M G Butler
Journal:  Med Anthropol       Date:  1989-04

3.  Metacarpophalangeal pattern profile analysis in clinical genetics: an applied anthropometric method.

Authors:  M G Butler; F J Meaney; S G Kaler
Journal:  Am J Phys Anthropol       Date:  1986-06       Impact factor: 2.868

4.  Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome.

Authors:  M G Butler; F J Meaney; C G Palmer
Journal:  Am J Med Genet       Date:  1986-03

5.  Metacarpophalangeal pattern profile analysis in Sotos syndrome.

Authors:  M G Butler; F J Meaney; S Kittur; J H Hersh; L Hornstein
Journal:  Am J Med Genet       Date:  1985-04

6.  Prader-Willi Syndrome: Clinical and Genetic Findings.

Authors:  Merlin G Butler; Travis Thompson
Journal:  Endocrinologist       Date:  2000-07

7.  Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment.

Authors:  M Fraccaro; O Zuffardi; E Bühler; A Schinzel; G Simoni; R Witkowski; E Bonifaci; D Caufin; G Cignacco; N Delendi
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

8.  Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes.

Authors:  E Roof; W Stone; W MacLean; I D Feurer; T Thompson; M G Butler
Journal:  J Intellect Disabil Res       Date:  2000-02

9.  Unbalanced reciprocal translocations in cases of Prader-Willi syndrome.

Authors:  D P Duckett; S H Roberts; P Davies
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

10.  Prader-Willi syndrome: current understanding of cause and diagnosis.

Authors:  M G Butler
Journal:  Am J Med Genet       Date:  1990-03
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