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Spontaneous repigmentation of silvery hair in an infant with congenital hydrops fetalis and hypoproteinemia.
Cutis. 2016 Jun;97(6):E1-5.
Cutis. 2016.
PMID: 27416089
dup(1)(q21q32) as a sole cytogenetic event is associated to a leukemic transformation in myelodysplastic syndromes.
Alfaro R, Pérez-Granero A, Durán MA, Besalduch J, Rosell J, Bernués M.
Alfaro R, et al. Among authors: perez granero a.
Leuk Res. 2008 Jan;32(1):159-61. doi: 10.1016/j.leukres.2007.03.033. Epub 2007 May 16.
Leuk Res. 2008.
PMID: 17509681
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Mutations in TBX1 genocopy the 22q11.2 deletion and duplication syndromes: a new susceptibility factor for mental retardation.
Torres-Juan L, Rosell J, Morla M, Vidal-Pou C, García-Algas F, de la Fuente MA, Juan M, Tubau A, Bachiller D, Bernues M, Perez-Granero A, Govea N, Busquets X, Heine-Suñer D.
Torres-Juan L, et al. Among authors: perez granero a.
Eur J Hum Genet. 2007 Jun;15(6):658-63. doi: 10.1038/sj.ejhg.5201819. Epub 2007 Mar 21.
Eur J Hum Genet. 2007.
PMID: 17377518
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Gene symbol: SRY.
Heine-Suñer D, Torres-Juan L, Gómez C, Pérez-Granero A, Bernues M, Govea N, Roseli J.
Heine-Suñer D, et al. Among authors: perez granero a.
Hum Genet. 2007 Feb;120(6):909.
Hum Genet. 2007.
PMID: 17438599
No abstract available.
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Unrelated chromosomal anomalies found in patients with suspected 22q11.2 deletion.
Fernández L, Lapunzina P, Pajares IL, Palomares M, Martínez I, Fernández B, Quero J, García-Guereta L, García-Alix A, Burgueros M, Galán-Gómez E, Carbonell-Pérez JM, Pérez-Granero A, Torres-Juan L, Heine-Suñer D, Rosell J, Delicado A.
Fernández L, et al. Among authors: perez granero a.
Am J Med Genet A. 2008 May 1;146A(9):1134-41. doi: 10.1002/ajmg.a.32256.
Am J Med Genet A. 2008.
PMID: 18384142
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