Criado GR - Search Results

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Higher frequency of uncommon 1.5-2 Mb deletions found in familial cases of 22q11.2 deletion syndrome.

Fernández L, Lapunzina P, Pajares IL, Criado GR, García-Guereta L, Pérez J, Quero J, Delicado A. Fernández L, et al. Among authors: criado gr. Am J Med Genet A. 2005 Jul 1;136(1):71-5. doi: 10.1002/ajmg.a.30756. Am J Med Genet A. 2005. PMID: 15889418

Möbius sequence, hypogenitalism, cerebral, and skeletal malformations in two brothers.

Criado GR, Aytés AP. Criado GR, et al. Am J Med Genet. 1999 Oct 29;86(5):492-6. doi: 10.1002/(sici)1096-8628(19991029)86:5<492::aid-ajmg17>3.0.co;2-e. Am J Med Genet. 1999. PMID: 10508994

Infantile systemic hyalinosis: a clinicopathological study.

Criado GR, González-Meneses A, Cañadas M, Rafel E, Yanes F, De Terreros IG. Criado GR, et al. Am J Med Genet A. 2004 Sep 1;129A(3):282-5. doi: 10.1002/ajmg.a.30117. Am J Med Genet A. 2004. PMID: 15326628

Characterization of the sialidase molecular defects in sialidosis patients suggests the structural organization of the lysosomal multienzyme complex.

Lukong KE, Elsliger MA, Chang Y, Richard C, Thomas G, Carey W, Tylki-Szymanska A, Czartoryska B, Buchholz T, Criado GR, Palmeri S, Pshezhetsky AV. Lukong KE, et al. Among authors: criado gr. Hum Mol Genet. 2000 Apr 12;9(7):1075-85. doi: 10.1093/hmg/9.7.1075. Hum Mol Genet. 2000. PMID: 10767332

[Ethiology and pathology of low birth weight infants in our hospital (author's transl)].

Díez FJ, Gómez SR, Criado GR, Hernández AP, Cuevas GP, Pardo A, De Llano MR. Díez FJ, et al. Among authors: criado gr. An Esp Pediatr. 1975 Jun;8 Suppl 1:1-12. An Esp Pediatr. 1975. PMID: 1155870 Spanish.

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