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1.
Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagia.
Am J Med Genet A
; 152A(1): 102-10, 2010 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-20034100
2.
A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity.
Eur J Med Genet
; 49(4): 298-305, 2006.
Artículo
en Inglés
| MEDLINE | ID: mdl-16829351
3.
Molecular cytogenetic characterization of an inherited maternal duplication 20p11.21p13 associated with a small 20p11.21 deletion.
Am J Med Genet A
; 152A(12): 3197-202, 2010 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-21108409
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