subject area of
- 4.3‐Mb triplication of 4q32.1–q32.2: Report of a family through two generations Journal Articles
- A rare subtelomeric deletion syndrome: Wolf Hirschhorn syndrome. Journal Articles
- An inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene cluster Journal Articles
- Clinical features of facioscapulohumeral muscular dystrophy 2 Journal Articles
- Deletion 4q21/4q22 syndrome: Two patients with de novo 4q21.3q23 and 4q13.2q23 deletions Journal Articles
- Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium Journal Articles
- Wolf-Hirschorn syndrome resulting from partial monosomy 4p/trisomy 9p Journal Articles