Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2.

Biancalana, V

Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2. [electronic resource] - American journal of human genetics May 1992 - 981-7 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

0002-9297


Abnormalities, Multiple--genetics
Female
Genetic Linkage--genetics
Genetic Markers--genetics
Humans
Intellectual Disability--genetics
Male
Mutation--genetics
Pedigree
Polymorphism, Restriction Fragment Length
Syndrome
X Chromosome