RDCI, the vasoactive intestinal peptide receptor: a candidate gene for the features of Albright hereditary osteodystrophy associated with deletion of 2q37.

Author:

Power M M,James R S,Barber J C,Fisher A M,Wood P J,Leatherdale B A,Flanagan D E,Hatchwell E

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference25 articles.

1. Pseudohypoparathyroidism: an example of "Seabright-Bantam syndrome";Albright, F.; Burnett, C.H.; Parson, W.;Endocrinology,1942

2. Albright F, Forbes AP, Henneman PH. Pseudopseudohypoparathyroidism. Trans Assoc Am Physicians 1952;65:337-50.

3. Albright hereditary osteodystrophy and del(2)(q37.3) in four unrelated individuals;Phelan, M.C.; Curtis Rogers, R.; Clarkson, K.B.;Am J Med Genet,1995

4. Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localised to 2q37;Wilson, L.C.; Leverton, K.; Oude Luttikhuis, M.E.M.;Am J Hum Genet,1995

5. Microdeletion in chromosome 2qter in two unrelated children with characteristic facies and mental retardation;Haag, M.; Gilfillan, T.; Berry, R.;Am J Hum Genet,1993

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