Identification of new mutations in the TBX5 gene in patients with Holt-Oram syndrome.

Heinritz, W

Identification of new mutations in the TBX5 gene in patients with Holt-Oram syndrome. [electronic resource] - Heart (British Cardiac Society) Mar 2005 - 383-4 p. digital

Publication Type: Letter

1468-201X

10.1136/hrt.2004.036855 doi


Adolescent
Adult
Arm--abnormalities
Child, Preschool
Chromosomes, Human, Pair 12--genetics
DNA--analysis
Family Health
Female
Heart Defects, Congenital--genetics
Humans
Male
Middle Aged
Mutation--genetics
Phenotype
Sequence Analysis, DNA--methods
Syndrome
T-Box Domain Proteins--genetics