González-Del Angel A - Search Results

1

Further delineation of achondroplasia-hypochondroplasia complex with long-term survival.

González-Del Angel A, Rius R, Alcántara-Ortigoza MA, Spector E, Del Castillo V, Mata-García LE. González-Del Angel A, et al. Am J Med Genet A. 2018 May;176(5):1225-1231. doi: 10.1002/ajmg.a.38660. Am J Med Genet A. 2018. PMID: 29681095 Review.

2

[Identification of sex chromosome markers using fluorescence in situ hybridization (FISH)].

González-del-Angel A, Blanco B, del Castillo V, Carnevale A. González-del-Angel A, et al. Rev Invest Clin. 1995 Mar-Apr;47(2):117-25. Rev Invest Clin. 1995. PMID: 7610280 Spanish.

3

Renal tubular acidosis in the Silver-Russell syndrome.

Alvarenga R, González del Angel A, del Castillo V, García de la Puente S, Maulén I, Carnevale A. Alvarenga R, et al. Am J Med Genet. 1995 Mar 27;56(2):173-5. doi: 10.1002/ajmg.1320560212. Am J Med Genet. 1995. PMID: 7625441

4

Microtia: a clinical and genetic study at the National Institute of Pediatrics in Mexico City.

Llano-Rivas I, González-del Angel A, del Castillo V, Reyes R, Carnevale A. Llano-Rivas I, et al. Arch Med Res. 1999 Mar-Apr;30(2):120-4. doi: 10.1016/s0188-0128(98)00023-2. Arch Med Res. 1999. PMID: 10372445

5

Ataxia-pancytopenia syndrome.

González-del Angel A, Cervera M, Gómez L, Pérez-Vera P, Orozco L, Carnevale A, Del Castillo V. González-del Angel A, et al. Am J Med Genet. 2000 Jan 31;90(3):252-4. doi: 10.1002/(sici)1096-8628(20000131)90:3<252::aid-ajmg14>3.3.co;2-m. Am J Med Genet. 2000. PMID: 10678666

6

Molecular diagnosis of the fragile X and FRAXE syndromes in patients with mental retardation of unknown cause in Mexico.

González-del Angel A, Vidal S, Saldaña Y, del Castillo V, Angel Alcántara M, Macías M, Pedro Luna J, Orozco L. González-del Angel A, et al. Ann Genet. 2000 Jan-Mar;43(1):29-34. doi: 10.1016/s0003-3995(00)00018-6. Ann Genet. 2000. PMID: 10818218

7

Trisomy of the short arm of chromosome 5 due to a de novo inversion and duplication (5)(p15.3 p13.3).

Cervera M, Sánchez S, Molina B, Alcántara MA, Del Castillo V, Carnevale A, González-del Angel A. Cervera M, et al. Am J Med Genet A. 2005 Aug 1;136A(4):381-5. doi: 10.1002/ajmg.a.30791. Am J Med Genet A. 2005. PMID: 16001443 Review.

8

Analysis of the CTNS gene in nephropathic cystinosis Mexican patients: report of four novel mutations and identification of a false positive 57-kb deletion genotype with LDM-2/exon 4 multiplex PCR assay.

Alcántara-Ortigoza MA, Belmont-Martínez L, Vela-Amieva M, González-Del Angel A. Alcántara-Ortigoza MA, et al. Genet Test. 2008 Sep;12(3):409-14. doi: 10.1089/gte.2008.0014. Genet Test. 2008. PMID: 18752449

9

Molecular analysis of the PAX6 gene in Mexican patients with congenital aniridia: report of four novel mutations.

Villarroel CE, Villanueva-Mendoza C, Orozco L, Alcántara-Ortigoza MA, Jiménez DF, Ordaz JC, González-del Angel A. Villarroel CE, et al. Mol Vis. 2008 Sep 8;14:1650-8. Mol Vis. 2008. PMID: 18776953 Free PMC article.

10

Kapur-Toriello syndrome: further delineation.

Yokoyama E, Martínez A, González-Del Angel A. Yokoyama E, et al. Am J Med Genet A. 2008 Nov 1;146A(21):2791-3. doi: 10.1002/ajmg.a.32369. Am J Med Genet A. 2008. PMID: 18831061

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