Familial inv(1)(p36.3q12) associated with sterility.
AUTOR(ES)
Barros, A
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1049552Documentos Relacionados
- Molecular-cytogenetic detection of a deletion of 1p36.3.
- Familial pericentric inversion inv(8)(p23q11).
- Rubinstein-Taybi syndrome: a female patient with a de novo reciprocal translocation t(2; 16)(q36.3; p13.3) and dysgranulopoiesis
- Pericentric inversion inv(3)(p11q21).
- Familial mental retardation associated with balanced chromosome rearrangement rcp t(8;11)(q24.3;p15.1).