Related Experiment Videos

A heritable fragile 12q24.13 segregating in a family with the fragile X chromosome

A P Amarose, P R Huttenlocher, R M Sprudzs

|January 1, 1987

Abstract:

A fragile site on chromosome 12, at 12q24.13, was found in the lymphocytes of two members of a family during the study for detection of a fragile X chromosome. The site was found to be heritable and folate-sensitive, and it fulfills all four criteria for a fragile site. It thus can now be confirmed as the heritable fragile site FRA12C.

Related Concept Videos

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

Ring chromosome 17: phenotype variation by deletion size.

Clinical genetics·2003

A family with seizures and minor features of tuberous sclerosis and a novel TSC2 mutation.

Neurology·2003

Fatal EBV-related post-transplant lymphoproliferative disorder (LPD) after matched related donor nonmyeloablative peripheral blood progenitor cell transplant.

Bone marrow transplantation·2003

Biochemical and mutational analyses of the cathepsin c gene (CTSC) in three North American families with Papillon Lefèvre syndrome.

Human mutation·2002

Localization, genomic organization, and alternative transcription of a novel human SAM-dependent methyltransferase gene on chromosome 2p22-->p21.

Cytogenetics and cell genetics·2002

Primary malignant lymphoma of uterine corpus: case report and review of the literature.

Annals of hematology·2002

See all related articles