Ramírez-Dueñas ML - Search Results

1

Severe Craniofacial Involvement due to Amniotic Band Sequence.

Becerra-Solano LE, Castañeda-Cisneros G, Corona-Rivera JR, Díaz-Rodríguez M, Figuera LE, López-Muñoz E, Nastasi-Catanese JA, Toscano-Flores JJ, Ramírez-Dueñas ML, García-Ortíz JE. Becerra-Solano LE, et al. Among authors: ramirez duenas ml. Fetal Pediatr Pathol. 2018 Feb;37(1):27-37. doi: 10.1080/15513815.2017.1392663. Epub 2018 Jan 16. Fetal Pediatr Pathol. 2018. PMID: 29336649

2

Benign familial macrocephaly in a mother-son pair.

Díaz-Rodríguez M, Becerra-Solano LE, Toscano-Flores JJ, Bañuelos-Robles O, Durán-González J, Ramírez Dueñas ML. Díaz-Rodríguez M, et al. Among authors: ramirez duenas ml. Genet Couns. 2010;21(1):85-9. Genet Couns. 2010. PMID: 20420034

3

Schilbach-Rott syndrome in a third family: further delineation of an autosomal dominant trait.

Becerra-Solano LE, Casillas-Avila MP, Díaz-Rodríguez M, Nastasi-Catanese JA, Toscano-Flores JJ, Ramírez-Dueñas ML. Becerra-Solano LE, et al. Among authors: ramirez duenas ml. Genet Couns. 2007;18(3):317-23. Genet Couns. 2007. PMID: 18019373

4

A 9p13-->p24 duplication coupled with a whole 22q translocation onto 9p24.

Rivera H, Vásquez-Velásquez AI, Ramirez-Duenas Mde L, Becerra-Solano LE. Rivera H, et al. J Appl Genet. 2007;48(1):95-8. doi: 10.1007/BF03194665. J Appl Genet. 2007. PMID: 17272869

5

[True hermaphroditism and sequences. Diagnostic implications regarding two cases].

Toscano-Flores Jde J, Padilla-Gutiérrez J, Becerra-Solano L, Díaz-Rodríguez M, Bañuelos-Robles O, Rivas-Solís F, Ramírez-Dueñas Mde L. Toscano-Flores Jde J, et al. Rev Med Inst Mex Seguro Soc. 2008 Sep-Oct;46(5):539-42. Rev Med Inst Mex Seguro Soc. 2008. PMID: 19241663 Spanish.

6

Expanding the phenotype of spondylospinal thoracic dysostosis (the Turkel-Chen-Johnson syndrome).

Becerra-Solano LE, Chacon L, Morales-Mata D, Ramírez-Dueñas Mde L, García-Ortiz JE. Becerra-Solano LE, et al. Clin Dysmorphol. 2015 Jan;24(1):1-6. doi: 10.1097/MCD.0000000000000058. Clin Dysmorphol. 2015. PMID: 25304117

7

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

8

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

9

The variable phenotype in tetrasomy 18p syndrome. A propos of a subtle dysmorphic case.

Brambila Tapia AJ, Figuera L, Vázquez Cárdenas NA, Ramírez Torres V, Vázquez Velázquez AI, García Contreras C, Ramírez Dueñas ML. Brambila Tapia AJ, et al. Among authors: ramirez duenas ml. Genet Couns. 2010;21(3):277-83. Genet Couns. 2010. PMID: 20964117

10

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

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