García-Cruz D - Search Results

1

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. Br J Dermatol. 2005 Dec;153(6):1216-9. doi: 10.1111/j.1365-2133.2005.06958.x. Br J Dermatol. 2005. PMID: 16307662

2

Inherited hypertrichoses.

Garcia-Cruz D, Figuera LE, Cantu JM. Garcia-Cruz D, et al. Clin Genet. 2002 May;61(5):321-9. doi: 10.1034/j.1399-0004.2002.610501.x. Clin Genet. 2002. PMID: 12081714 Review.

3

Molecular characterization of the fragile-X syndrome in the Mexican population.

Díaz-Gallardo MY, Barros-Núñez P, Díaz CA, Hernández A, Gómez-Espinel I, Leal CA, Fragoso R, Figuera L, García-Cruz D, Ramírez-Dueñas ML. Díaz-Gallardo MY, et al. Arch Med Res. 1995;26 Spec No:S77-83. Arch Med Res. 1995. PMID: 8845662

4

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. Genet Couns. 2003;14(1):31-7. Genet Couns. 2003. PMID: 12725587

5

Guadalajara camptodactyly syndrome type I. A corroborative family.

Figuera LE, Ramírez-Dueñas ML, García-Cruz D, Villar V, Cantú JM. Figuera LE, et al. Clin Genet. 1993 Jan;43(1):11-5. doi: 10.1111/j.1399-0004.1993.tb04418.x. Clin Genet. 1993. PMID: 7681735

6

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

7

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

8

Del Xq23 in a mosaic Turner female: molecular and cytogenetic studies.

Mesa-Cornejo VM, García-Cruz D, Monroy-Jaramillo N, Vásquez AI, Dávalos NO, Galaviz C, Kofman S. Mesa-Cornejo VM, et al. Ann Genet. 2001 Oct-Dec;44(4):171-4. doi: 10.1016/s0003-3995(01)01092-9. Ann Genet. 2001. PMID: 11755099

9

The Myhre syndrome: report of two cases.

García-Cruz D, Figuera LE, Feria-Velazco A, Sánchez-Corona J, García-Cruz MO, Ramírez-Duenãs RM, Hernandez-Córdova A, Ruiz MX, Bitar-Alatorre WE, Ramírez-Dueñas ML, et al. García-Cruz D, et al. Clin Genet. 1993 Oct;44(4):203-7. doi: 10.1111/j.1399-0004.1993.tb03880.x. Clin Genet. 1993. PMID: 8261650

10

Ring-20-syndrome and loss of telomeric regions.

García-Cruz D, Vásquez AI, Perez-Rulfo D, Dávalos NO, Peñaloza J, García-Ortiz JE, Patiño-García B, Sánchez-Corona J. García-Cruz D, et al. Ann Genet. 2000 Jul-Dec;43(3-4):113-6. doi: 10.1016/s0003-3995(00)01027-3. Ann Genet. 2000. PMID: 11164191

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