Mayén Molina DG - Search Results

1

[Prenatal molecular diagnosis of a DMD carrier female fetus by chorionic villus sampling and linkage analysis].

Alcántara Ortigoza MA, Aguinaga Ríos M, González del Angel A, Zavaleta Abreu Mde J, Acevedo Gallegos S, Mayén Molina DG, del Castillo Ruíz V. Alcántara Ortigoza MA, et al. Among authors: mayen molina dg. Ginecol Obstet Mex. 2009 Feb;77(2):103-9. Ginecol Obstet Mex. 2009. PMID: 19365952 Review. Spanish.

2

[Genetic counseling in perinatal field].

Mayén Molina DG, Baez Reyes Mdel R, Grether González P, Aizpuru Akel E, Aguinaga Ríos M, García Cavazos R, Gómez Arteaga GM; Colegio Mexicano de Especialistas en Ginecología y Obstetricia. Mayén Molina DG, et al. Ginecol Obstet Mex. 2009 Jan;77(1):S1-25. Ginecol Obstet Mex. 2009. PMID: 19365961 Spanish. No abstract available.

3

[Attitude to and acceptance of prenatal cytogenetic diagnosis by pregnant women].

Mayén-Molina DG, Hernández-González C, Grether-González P. Mayén-Molina DG, et al. Ginecol Obstet Mex. 1997 Mar;65:107-10. Ginecol Obstet Mex. 1997. PMID: 9190352 Spanish.

4

[Abnormalities of sex chromosomes and relationship with reproduction disorders].

Baez-Reyes MR, Mayen-Molina DG, Zavaleta-Abreu MJ, García-Cavazos RJ. Baez-Reyes MR, et al. Among authors: mayen molina dg. Ginecol Obstet Mex. 1998 Sep;66:367-70. Ginecol Obstet Mex. 1998. PMID: 9789409 Spanish.

5

[Non invasive prenatal test (NIPT) in maternal blood by parallel massive sequencing. Initial experience in Mexican women and literature review].

Hernández-Gómez M, Ramirez-Arroyo E, Meléndez-Hernández R, Garduño-Zaraza LM, Mayén-Molina DG. Hernández-Gómez M, et al. Among authors: mayen molina dg. Ginecol Obstet Mex. 2015 May;83(5):277-88. Ginecol Obstet Mex. 2015. PMID: 26233973 Review. Spanish.

6

Prenatal diagnosis of trisomy 21 without the Down syndrome phenotype.

Aguinaga M, Razo G, Castro J, Mayén-Molina DG. Aguinaga M, et al. Among authors: mayen molina dg. Prenat Diagn. 2006 Dec;26(12):1168-71. doi: 10.1002/pd.1583. Prenat Diagn. 2006. PMID: 17042031

7

Partial trisomy 9: prenatal diagnosis and recurrence within same family.

López-Félix J, Flores-Gallegos L, Garduño-Zarazúa L, Leis-Márquez T, Juárez-García L, Meléndez-Hernández R, Castelazo-Morales E, Mayén-Molina D. López-Félix J, et al. Clin Case Rep. 2017 May 10;5(6):986-992. doi: 10.1002/ccr3.970. eCollection 2017 Jun. Clin Case Rep. 2017. PMID: 28588852 Free PMC article.

8

[Recurrent aneuploidy in first trimester gestational loss: a case report and review of the literature].

Hernández-Gómez M, Meléndez-Hernández R, Rojas-Saiz WH, Maya-Goldsmit D, Mayén-Molina DG. Hernández-Gómez M, et al. Among authors: mayen molina dg. Ginecol Obstet Mex. 2013 Dec;81(12):733-7. Ginecol Obstet Mex. 2013. PMID: 24620528 Review. Spanish.

9

Prenatal clinical characteristics of Casamassima-Morton-Nance syndrome.

Aguinaga M, Yllescas E, Canseco M, Machuca A, Acevedo S, Mayén Molina DG. Aguinaga M, et al. Among authors: mayen molina dg. Prenat Diagn. 2009 Feb;29(2):175-6. doi: 10.1002/pd.2168. Prenat Diagn. 2009. PMID: 19090487 No abstract available.

10

Facial anthropometric measurements in offspring of epileptic mothers.

Díaz-Romero RM, Garza-Morales S, Mayén-Molina DG, Ibarra-Puig J, Avila-Rosas H. Díaz-Romero RM, et al. Among authors: mayen molina dg. Arch Med Res. 1999 May-Jun;30(3):186-9. doi: 10.1016/s0188-0128(99)00007-x. Arch Med Res. 1999. PMID: 10427868

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