Literature DB >> 2303250

Growth retardation in Wolf-Hirschhorn syndrome.

A Fujimoto1, M G Wilson.   

Abstract

Postnatal growth records of 13 patients with Wolf-Hirschhorn syndrome indicate that the syndrome is associated with continuing severe growth retardation and marked microcephaly. In spite of severe retardation, these patients (with one exception) survived beyond infancy.

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Year:  1990        PMID： 2303250     DOI： 10.1007/bf00200580

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  3 in total

1.  Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion.

Authors:  K Hirschhorn; H L Cooper; I L Firschein
Journal:  Humangenetik       Date:  1965

2.  [Deficiency on the short arms of a chromosome No. 4].

Authors:  U Wolf; H Reinwein; R Porsch; R Schröter; H Baitsch
Journal:  Humangenetik       Date:  1965

3.  Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)].

Authors:  M G Wilson; J W Towner; G S Coffin; A J Ebbin; E Siris; P Brager
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
  3 in total
  2 in total

1.  A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation.

Authors:  J Goodship; A Curtis; I Cross; J Brown; J Emslie; J Wolstenholme; S Bhattacharya; J Burn
Journal:  J Med Genet       Date:  1992-07       Impact factor: 6.318

2.  A complex rearrangement associated with sex reversal and the Wolf-Hirschhorn syndrome: a cytogenetic and molecular study.

Authors:  K Coles; M Mackenzie; J Crolla; J Harvey; J Starr; F Howard; P Jacobs
Journal:  J Med Genet       Date:  1992-06       Impact factor: 6.318
  2 in total

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