Related Experiment Videos

On the gates of hell and a most unusual gene

American Journal of Medical Genetics

|January 1, 1986

Abstract

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

A de novo splice site mutation in CASK causes FG syndrome-4 and congenital nystagmus.

American journal of medical genetics. Part A·2017

Simpson-Golabi-Behmel syndrome: an X-linked encephalo-tropho-schisis syndrome. 1988.

American journal of medical genetics. Part A·2013

The cardiofaciocutaneous syndrome.

Journal of medical genetics·2006

"Double-muscle" trait in cattle: a possible model for Wiedemann-Beckwith syndrome.

Fetal and pediatric pathology·2006

Absence of 12q21.2q22 deletions and subtelomeric rearrangements in cardiofaciocutaneous (CFC) syndrome patients.

American journal of medical genetics. Part A·2003

PTPN11 mutations are not responsible for the Cardiofaciocutaneous (CFC) syndrome.

European journal of human genetics : EJHG·2003

See all related articles