Family Study of Inherited Syndrome With Multiple Congenital Deformities: Symphalangism, Carpal and Tarsal Fusion, Brachydactyly, Craniosynostosis, Strabismus, Hip Osteochondritis.

Journal of Medical Genetics - United Kingdom
doi 10.1136/jmg.13.5.394
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

BMJ

Related search

A Family Study of Craniosynostosis, With Probable Recognition of a Distinct Syndrome.

Journal of Medical Genetics
Genetics
1982English

Liebenberg Syndrome: Brachydactyly With Joint Dysplasia (MIM 186550): A Second Family

Journal of Medical Genetics
Genetics
2000English

Another “Multiple Congenital Anomalies” Syndrome - The W. Family

Pediatric Research
Child HealthPediatricsPerinatology
1974English

Unknown Syndrome: Congenital Heart Disease, Ptosis, Hypodontia, and Craniosynostosis.

Journal of Medical Genetics
Genetics
1989English

Congenital Deformities

Postgraduate Medical Journal
Medicine
1964English

A Novel R486Q Mutation in BMPR1B Resulting in Either a Brachydactyly Type C/Symphalangism-Like Phenotype or Brachydactyly Type A2

European Journal of Human Genetics
Genetics
2006English

Registration of Congenital Deformities

BMJ
1962English

Temtamy Preaxial Brachydactyly Syndrome

2020English

Congenital Deformities of Hands and Feet

BMJ
1938English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy