Familial combination of brachydactyly, type E and atrial septal defect, type II

E. Czeizel, P. Göblyös

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Nine members of a three generation family were affected with the combination of brachydactyly, type E and heart defect, mainly atrial septal defect, type II. A similar malformation pattern of autosomal dominant origin has not previously been delineated.

Original languageEnglish
Pages (from-to)117-119
Number of pages3
JournalEuropean Journal of Pediatrics
Volume149
Issue number2
DOIs
Publication statusPublished - Nov 1989

Fingerprint

Atrial Heart Septal Defects
Type E Brachydactyly

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Familial combination of brachydactyly, type E and atrial septal defect, type II. / Czeizel, E.; Göblyös, P.

In: European Journal of Pediatrics, Vol. 149, No. 2, 11.1989, p. 117-119.

Research output: Contribution to journalArticle

@article{ed133abfd8d04bc1aa778e8089255a6a,
title = "Familial combination of brachydactyly, type E and atrial septal defect, type II",
abstract = "Nine members of a three generation family were affected with the combination of brachydactyly, type E and heart defect, mainly atrial septal defect, type II. A similar malformation pattern of autosomal dominant origin has not previously been delineated.",
author = "E. Czeizel and P. G{\"o}bly{\"o}s",
year = "1989",
month = "11",
doi = "10.1007/BF01995860",
language = "English",
volume = "149",
pages = "117--119",
journal = "European Journal of Pediatrics",
issn = "0340-6199",
publisher = "Springer Verlag",
number = "2",

}

TY - JOUR

T1 - Familial combination of brachydactyly, type E and atrial septal defect, type II

AU - Czeizel, E.

AU - Göblyös, P.

PY - 1989/11

Y1 - 1989/11

N2 - Nine members of a three generation family were affected with the combination of brachydactyly, type E and heart defect, mainly atrial septal defect, type II. A similar malformation pattern of autosomal dominant origin has not previously been delineated.

AB - Nine members of a three generation family were affected with the combination of brachydactyly, type E and heart defect, mainly atrial septal defect, type II. A similar malformation pattern of autosomal dominant origin has not previously been delineated.

UR - http://www.scopus.com/inward/record.url?scp=0024329251&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0024329251&partnerID=8YFLogxK

U2 - 10.1007/BF01995860

DO - 10.1007/BF01995860

M3 - Article

VL - 149

SP - 117

EP - 119

JO - European Journal of Pediatrics

JF - European Journal of Pediatrics

SN - 0340-6199

IS - 2

ER -