Ramírez-Dueñas ML - Search Results

1

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

2

Spondyloepimetaphyseal dysplasia (SEMD) Shohat type.

Figuera LE, Ramírez-Dueñas ML, Gallegos-Arreola MP, Cantú JM. Figuera LE, et al. Am J Med Genet. 1994 Jul 1;51(3):213-5. doi: 10.1002/ajmg.1320510307. Am J Med Genet. 1994. PMID: 8074146

3

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

4

Kaufman oculocerebrofacial syndrome: report of two new cases and further delineation.

Figuera LE, García-Cruz D, Ramírez-Dueñas ML, Rivera-Robles V, Cantù JM. Figuera LE, et al. Clin Genet. 1993 Aug;44(2):98-101. doi: 10.1111/j.1399-0004.1993.tb03855.x. Clin Genet. 1993. PMID: 8275567

5

Are the faciothoracoskeletal syndrome and the Guadalajara camptodactyly syndrome type I distinct entities?

Ramírez-Dueñas ML, Cantú JM. Ramírez-Dueñas ML, et al. Am J Med Genet. 1995 Sep 11;58(3):293-4. doi: 10.1002/ajmg.1320580319. Am J Med Genet. 1995. PMID: 8533835 No abstract available.

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: ramirez duenas ml. Clin Dysmorphol. 2002 Oct;11(4):243-7. doi: 10.1097/00019605-200210000-00003. Clin Dysmorphol. 2002. PMID: 12401988

7

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

8

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

9

[Genetically caused deafness: prospective study of 109 children in a special school].

Ramírez-Dueñas ML, Ramírez-Dueñas MC, Matute E, Cantú JM. Ramírez-Dueñas ML, et al. Arch Invest Med (Mex). 1990 Oct-Dec;21(4):299-303. Arch Invest Med (Mex). 1990. PMID: 1669217 Spanish.

10

Opposite imbalances of distal 14q in two unrelated patients.

Rivera H, Ramirez-Dueñas ML, Figuera LE, Gonzalez-Montes RM, Vasquez AI. Rivera H, et al. Ann Genet. 1992;35(2):97-100. Ann Genet. 1992. PMID: 1524416

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