Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype-Reference-Cited by-同舟云学术

Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype

Published:2014-01-30 Issue:1 Volume:15 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Stagi Stefano,Lapi Elisabetta,Pantaleo Marilena,Chiarelli Francesco,Seminara Salvatore,de Martino Maurizio

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/1471-2350-15-16.pdf

Reference29 articles.

1. Shapira SK, McCaskill C, Northrup H, Spikes AS, Elder FF, Sutton VR, Korenberg JR, Greenberg F, Shaffer LG: Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome. Am J Hum Genet. 1997, 61: 642-650. 10.1086/515520.

2. Heilstedt HA, Ballif BC, Howard LA, Kashorf CD, Shaffer LG: Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality. Clin Genet. 2003, 64: 310-316. 10.1034/j.1399-0004.2003.00126.x.

3. Battaglia A, Hoyme HE, Dallapiccola B, Zackai E, Hudgins L, McDonald-McGinn D, Bahi-Buisson N, Romano C, Williams CA, Brailey LL, Zuberi SM, Carey JC: Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation. Pediatrics. 2008, 121: 404-410. 10.1542/peds.2007-0929.

4. Gajecka M, Mackay KL, Shaffer LG: Monosomy 1p36 deletion syndrome. Am J Med Genet C: Semin Med Genet. 2007, 145C: 346-356. 10.1002/ajmg.c.30154.

5. Slavotinek A, Shaffer LG, Shapira SK: Monosomy 1p36. J Med Genet. 1999, 36: 657-663.

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