Figuera LE - Search Results

1

Interstitial deletion of 13q22-->q31: case report and review of the literature.

Morales JA, Mendizabal AP, Vásquez AI, Figuera LE, González-García JR. Morales JA, et al. Among authors: figuera le. Clin Dysmorphol. 2006 Jul;15(3):139-143. doi: 10.1097/01.mcd.0000204990.46743.7b. Clin Dysmorphol. 2006. PMID: 16760731 Review.

2

Translocation/duplication of 9p onto a duplicated 4q.

Rivera H, Figuera LE, Vasquez AI. Rivera H, et al. Among authors: figuera le. Genet Couns. 1992;3(4):201-3. Genet Couns. 1992. PMID: 1472355

3

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. Among authors: figuera le. Ann Genet. 1992;35(2):97-100. Ann Genet. 1992. PMID: 1524416

4

Interstitial deletion 6q16.2q22.2 in a child with ectrodactyly.

Correa-Cerro L, Garcíaz-Cruz D, Díaz-Castaños L, Figuera LE, Sanchez-Corona J. Correa-Cerro L, et al. Among authors: figuera le. Ann Genet. 1996;39(2):105-9. Ann Genet. 1996. PMID: 8766142

5

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

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

6

Pure partial trisomy 6p due to a familial insertion (16;6)(p12;p21.2p23).

Domínguez MG, Wong-Ley LE, Rivera H, Vásquez AI, Ramos AL, Sánchez-Urbina R, Morales JA, Figuera LE. Domínguez MG, et al. Among authors: figuera le. Ann Genet. 2003 Jan-Mar;46(1):45-8. doi: 10.1016/s0003-3995(03)00004-2. Ann Genet. 2003. PMID: 12818529

7

First case reported of Turner syndrome and trisomy 14 chromosomal mosaicism in a patient.

Becerra-Solano LE, Arnaud-Lopez L, Diaz-Rodriguez M, Mantilla-Capacho JM, Nastasi-Catanese JA, Ortiz-Aranda M, Vasquez AI, Figuera LE. Becerra-Solano LE, et al. Among authors: figuera le. Clin Dysmorphol. 2008 Jan;17(1):27-30. doi: 10.1097/MCD.0b013e3282ef947d. Clin Dysmorphol. 2008. PMID: 18049077

8

Distribution of CYP1A1*2A polymorphism in adult patients with acute lymphoblastic leukemia in a Mexican population.

Gallegos-Arreola MP, González-García JR, Figuera LE, Puebla-Pérez AM, Delgado-Lamas JL, Zúñiga-González GM. Gallegos-Arreola MP, et al. Among authors: figuera le. Blood Cells Mol Dis. 2008 Jul-Aug;41(1):91-4. doi: 10.1016/j.bcmd.2007.12.001. Epub 2008 Jan 18. Blood Cells Mol Dis. 2008. PMID: 18203634

9

The fifth female patient with Myhre syndrome: further delineation.

Becerra-Solano LE, Díaz-Rodriguez M, Nastasi-Catanese JA, Toscano-Flores JJ, Bañuelos-Robles O, Figuera LE, Matute E, de Lourdes Ramírez-Dueñas M. Becerra-Solano LE, et al. Among authors: figuera le. Clin Dysmorphol. 2008 Apr;17(2):113-117. doi: 10.1097/MCD.0b013e3282f52828. Clin Dysmorphol. 2008. PMID: 18388781

10

Two familial intrachromosomal insertions with maternal dup(6)(p22.3p25.3) or dup(2)(q24.2q32.1) in recombinant offspring.

Domínguez MG, Rivera H, Aguilar-Lemarroy A, Jave-Suarez LF, Ramírez-Velazco A, González-Ramos IA, Barros-Núñez P, Partida-Pérez M, Gutiérrez-Amavizca BE, Brambila-Tapia AJ, Figuera LE. Domínguez MG, et al. Among authors: figuera le. Clin Dysmorphol. 2017 Oct;26(4):209-216. doi: 10.1097/MCD.0000000000000191. Clin Dysmorphol. 2017. PMID: 28737552

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