Literature DB >> 4809791

Variable expression of the Holt-Oram syndrome.

R L Kaufman, D L Rimoin, W H McAlister, A F Hartmann.   

Abstract

Mesh：

Year:  1974        PMID： 4809791     DOI： 10.1001/archpedi.1974.02110200023003

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN： 0002-922X


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  6 in total

1.  An operated case of Holt-Oram syndrome with autosomal dominant inheritance.

Authors:  Z Czakó; A Gömöry; P Homolay; S Bacsa; S Kiss; F Móricz; F Fülöp; Z Papp
Journal:  Basic Res Cardiol       Date:  1976 Jan-Feb       Impact factor: 17.165

Review 2.  Clues in diagnosing congenital heart disease.

Authors:  A J Moss
Journal:  West J Med       Date:  1992-04

3.  Brief clinical report: a child with radius aplasia, cleft of lip and palate, microcephaly, and unusual chromosome findings.

Authors:  M G Butler; L J Russell; C G Palmer; M Bull; M E Hodes
Journal:  Am J Med Genet       Date:  1982-12

4.  Holt Oram syndrome mistaken for thalidomide embryopathy--embryological considerations.

Authors:  N Van Regemorter; D Haumont; C Kirkpatrick; P Viseur; P Jeanty; J Dodion; J Milaire; M Rooze; F Rodesch
Journal:  Eur J Pediatr       Date:  1982-02       Impact factor: 3.183

Review 5.  Triphalangeal thumb.

Authors:  Q Qazi; E G Kassner
Journal:  J Med Genet       Date:  1988-08       Impact factor: 6.318

6.  Holt-Oram syndrome: a clinical genetic study.

Authors:  R A Newbury-Ecob; R Leanage; J A Raeburn; I D Young
Journal:  J Med Genet       Date:  1996-04       Impact factor: 6.318
  6 in total

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