Dávalos IP - Search Results

1

Zimmermann-Laband syndrome: further clinical delineation.

Dávalos IP, García-Cruz D, García-Cruz MO, Ramírez-Dueñas ML, Solis-Cámara P, Correa-Cerro LS, Perez-Rulfo D, Sánchez-Corona J. Dávalos IP, et al. Genet Couns. 2005;16(3):283-90. Genet Couns. 2005. PMID: 16261693

2

Floating-Harbor syndrome. A neuropsychological approach.

Davalos IP, Figuera LE, Bobadilla L, Martinez-Martinez R, Matute E, Partida MG, Bañuelos LA, Ramirez-Dueñas ML. Davalos IP, et al. Genet Couns. 1996;7(4):283-8. Genet Couns. 1996. PMID: 8985732

3

A variant example of familial Floating-Harbor syndrome?

Peñaloza JM, García-Cruz D, Dávalos IP, Dávalos NO, García-Cruz MO, Pérez-Rulfo D, Sánchez-Corona J. Peñaloza JM, et al. Among authors: davalos no, davalos ip. Genet Couns. 2003;14(1):31-7. Genet Couns. 2003. PMID: 12725587

4

Wide clinical spectrum in Zimmermann-Laband syndrome.

Davalos IP, Brambila-Tapia AJ, Dávalos NO, Durán-González J, González-Mercado MG, Cruz-Ramos JA, Ríos-González BE, E'vega R, Zavala-Cerna MG, García-Cruz MO, García-cruz D. Davalos IP, et al. Genet Couns. 2011;22(1):1-10. Genet Couns. 2011. PMID: 21614982

5

Microcephaly, distinctive facies, single atrium, postaxial polydactyly, skeletal defects and mental retardation: a new familial faciocardiomelic syndrome?

García-Ortiz JE, García-Cruz D, Dávalos IP, Nazará Z, García-Cruz MO, Castañeda V, Gutiérrez-Mendivil L, Sánchez-Corona J. García-Ortiz JE, et al. Among authors: davalos ip. Clin Dysmorphol. 2007 Jan;16(1):15-20. doi: 10.1097/01.mcd.0000198929.24577.a5. Clin Dysmorphol. 2007. PMID: 17159509

6

Guadalajara camptodactyly type III: a new probably autosomal dominant syndrome.

Figuera LE, Ramírez-Dueñas ML, Dávalos IP, Cantú JM. Figuera LE, et al. Among authors: davalos ip. Clin Dysmorphol. 2002 Oct;11(4):243-7. doi: 10.1097/00019605-200210000-00003. Clin Dysmorphol. 2002. PMID: 12401988

7

Alphoidless centromere of a familial unstable inverted Y chromosome.

Rivera H, Vassquez AI, Ayala-Madrigal ML, Ramirez-Dueñas ML, Davalos IP. Rivera H, et al. Among authors: davalos ip. Ann Genet. 1996;39(4):236-9. Ann Genet. 1996. PMID: 9037351

8

A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp.

Dávalos NO, García-Vargas A, Pforr J, Dávalos IP, Picos-Cárdenas VJ, García-Cruz D, Kruse R, Figuera LE, Nöthen MM, Betz RC. Dávalos NO, et al. Among authors: davalos ip. Br J Dermatol. 2005 Dec;153(6):1216-9. doi: 10.1111/j.1365-2133.2005.06958.x. Br J Dermatol. 2005. PMID: 16307662

9

Methylenetetrahydrofolate reductase C677T polymorphism and Factor V Leiden variant in Mexican women with preeclampsia/eclampsia.

Dávalos IP, Moran MC, Martínez-Abundis E, González-Ortiz M, Flores-Martínez SE, Machorro V, Sandoval L, Figuera LE, Mena JP, Oliva JM, Tlacuilo-Parra JA, Sánchez-Corona J, Salazar-Páramo M. Dávalos IP, et al. Blood Cells Mol Dis. 2005 Jul-Aug;35(1):66-9. doi: 10.1016/j.bcmd.2005.03.008. Blood Cells Mol Dis. 2005. PMID: 15905108

10

A de novo interstitial 6q deletion in a boy with a split hand malformation.

Duran-Gonzalez J, Gutierrez-Angulo M, Garcia-Cruz D, Ayala Mde L, Padilla M, Davalos IP. Duran-Gonzalez J, et al. Among authors: davalos ip. J Appl Genet. 2007;48(4):405-7. doi: 10.1007/BF03195240. J Appl Genet. 2007. PMID: 17998600

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