A. Cervantes

发表

19q13.11 microdeletion concomitant with ins(2;19)(p25.3;q13.1q13.4)dn in a boy: potential role of UBA2 in the associated phenotype

C. Venegas-Vega, J. Berumen, Karem Nieto-Martínez, 2014, Molecular Cytogenetics.

Liver disease in pregnancy: Medical aspects and their implications for mother and child.

C. Guzman, M. Cerbón, A. Cervantes, 2019, Annals of hepatology.

Genetic aspects in the medical approach of congenital heart defects

G. Queipo, F. Coronel-Cruz, A. Cervantes, 2020, Revista M�dica del Hospital General de M�xico.

PCR–PRINS–FISH analysis of structurally abnormal sex chromosomes in eight patients with Turner phenotype

S. Canún, C. Sierra, C. Navarrete, 2001, Clinical genetics.

Nance–Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature

J. Villa-Morales, Karem Nieto-Martínez, A. Martínez-Herrera, 2018, Ophthalmic genetics.

Microsatellite analysis in Turner syndrome: parental origin of X chromosomes and possible mechanism of formation of abnormal chromosomes.

S. Canún, J. Zenteno, Marisol López, 2002, American journal of medical genetics.

Frequency of Y chromosomal material in Mexican patients with Ullrich-Turner syndrome.

P. Canto, J. P. Méndez, A. Cervantes, 1998, American journal of medical genetics.

A mutation in the 5' non-high mobility group box region of the SRY gene in patients with Turner syndrome and Y mosaicism.

P. Canto, A. Ulloa-Aguirre, J. P. Méndez, 2000, The Journal of clinical endocrinology and metabolism.

Clinical traits and molecular findings in 46,XX males

R. Erickson, J. P. Méndez, Marisol López, 1995, Clinical genetics.

Molecular analysis in true hermaphrodites with different karyotypes and similar phenotypes.

R. Erickson, P. Canto, J. P. Méndez, 1996, American journal of medical genetics.

Mix Gonadal Dysgenesis Associated with Ring Y Chromosome Mosaics in a Phenotypic Male

G. Queipo, N. Nájera, A. Cervantes, 2009, Sexual Development.

Mutational spectrum of EDA and EDAR genes in a cohort of Mexican mestizo patients with hypohidrotic ectodermal dysplasia

M. Toledo-Bahena, M. López-López, M. Cerbón, 2017, Journal of the European Academy of Dermatology and Venereology : JEADV.

In vitro drug metabolism testing using blood-monocyte derivatives

I. González-Sánchez, M. Cerbón, G. Gómez-Icazbalceta, 2013, Expert opinion on drug metabolism & toxicology.

Trisomy 3q25.1‐qter and monosomy 8p23.1‐pter in a patient: Cytogenetic and molecular analysis with delineation of the phenotype

A. Saâd, C. Venegas-Vega, U. Friedrich, 2005, American journal of medical genetics. Part A.

Mosaic proximal trisomy 13q and regular trisomy 13 in a female patient with long survival: Involvement of an incomplete trisomic rescue and a chromothripsis event

A. Cervantes, Fernando Fernández-Ramírez, V. Morán-Barroso, 2021, Molecular genetics & genomic medicine.

Cytogenetic profile in 1,921 cases of trisomy 21 syndrome.

A. Cervantes, C. García-Delgado, V. Morán-Barroso, 2015, Archives of medical research.

Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes

J. Villa-Morales, J. Berumen, Karem Nieto-Martínez, 2014, BMC Medical Genomics.

Clinical, Cytogenetic, and Biochemical Analyses of a Family with a t(3;13)(q26.2;p11.2): Further Delineation of 3q Duplication Syndrome

A. Luna-Angulo, A. Cervantes, M. Abreu-González, 2013, Case reports in genetics.

Diagnosis of Familial Wolf-Hirschhorn Syndrome due to a Paternal Cryptic Chromosomal Rearrangement by Conventional and Molecular Cytogenetic Techniques

C. Venegas-Vega, J. Berumen, Karem Nieto-Martínez, 2013, BioMed research international.

Niemann-Pick disease A or B in four pediatric patients and SMPD1 mutation carrier frequency in the Mexican population.

P. Valencia-Mayoral, M. Cerbón, A. Ortega-Vázquez, 2019, Annals of hepatology.

HLA-DR4 and rheumatoid arthritis in Mexican mestizos.

A. Cervantes, G. Katona, V. Alvares, 1984, Arthritis and rheumatism.

Monosomy 9p24 in two non-related patients as result of a translocation (2;9).

A. Cervantes, C. Serrano-Bello, C. García-Delgado, 2018, Archivos Argentinos de Pediatria.

SRY alone can induce normal male sexual differentiation.

R. Erickson, J. P. Méndez, G. Pérez-palacios, 1995, American journal of medical genetics.

HLA and Heberden's nodes in Mexican Mestizos

A. Cervantes, G. Katona, G. Benavides, 1985, Clinical Rheumatology.

Congenital hypertrichosis universalis in Mexican female twins

A. Valencia-Herrera, A. Cervantes, S. Kofman, 2016, International journal of dermatology.