Recurrence of fibrochondrogenesis in a consanguineous family

L. I. Al-Gazali; M. Bakir; A. Dawodu; D. Haas

doi:10.1097/00019605-199901000-00011

Recurrence of fibrochondrogenesis in a consanguineous family

L. I. Al-Gazali, M. Bakir, A. Dawodu, D. Haas

Research output: Contribution to journal › Article › peer-review

8 Citations (Scopus)

Abstract

A second case of fibrochrondrogenesis in a consanguineous family is described. The fact that both sexes are affected in this family supports autosomal recessive inheritance.

Original language	English
Pages (from-to)	59-61
Number of pages	3
Journal	Clinical Dysmorphology
Volume	8
Issue number	1
DOIs	https://doi.org/10.1097/00019605-199901000-00011
Publication status	Published - 1999

Keywords

Autosomal recessive
Bone dysplasia
Lethal
Neonatal

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Anatomy
Pathology and Forensic Medicine
Genetics(clinical)

Access to Document

10.1097/00019605-199901000-00011

Cite this

@article{dd5aa9f2468a469792cdfc8bb04e46b5,

title = "Recurrence of fibrochondrogenesis in a consanguineous family",

abstract = "A second case of fibrochrondrogenesis in a consanguineous family is described. The fact that both sexes are affected in this family supports autosomal recessive inheritance.",

keywords = "Autosomal recessive, Bone dysplasia, Lethal, Neonatal",

author = "Al-Gazali, {L. I.} and M. Bakir and A. Dawodu and D. Haas",

year = "1999",

doi = "10.1097/00019605-199901000-00011",

language = "English",

volume = "8",

pages = "59--61",

journal = "Clinical Dysmorphology",

issn = "0962-8827",

publisher = "Lippincott Williams and Wilkins",

number = "1",

}

TY - JOUR

T1 - Recurrence of fibrochondrogenesis in a consanguineous family

AU - Al-Gazali, L. I.

AU - Bakir, M.

AU - Dawodu, A.

AU - Haas, D.

PY - 1999

Y1 - 1999

N2 - A second case of fibrochrondrogenesis in a consanguineous family is described. The fact that both sexes are affected in this family supports autosomal recessive inheritance.

AB - A second case of fibrochrondrogenesis in a consanguineous family is described. The fact that both sexes are affected in this family supports autosomal recessive inheritance.

KW - Autosomal recessive

KW - Bone dysplasia

KW - Lethal

KW - Neonatal

UR - http://www.scopus.com/inward/record.url?scp=0032968697&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0032968697&partnerID=8YFLogxK

U2 - 10.1097/00019605-199901000-00011

DO - 10.1097/00019605-199901000-00011

M3 - Article

C2 - 10327253

AN - SCOPUS:0032968697

SN - 0962-8827

VL - 8

SP - 59

EP - 61

JO - Clinical Dysmorphology

JF - Clinical Dysmorphology

IS - 1

ER -

Recurrence of fibrochondrogenesis in a consanguineous family

Abstract

Keywords

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this