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Polymorphisms C677T and A1298C in the MTHFR gene in Mexican patients with rheumatoid arthritis treated with methotrexate: implication with elevation of transaminases

The pharmacogenomics journal, 2011-08, Vol.11 (4), p.287-291

2011

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Association of the C677T polymorphism in the methylenetetrahydrofolate reductase gene with breast cancer in a Mexican population

Genetics and molecular research, 2015-04, Vol.14 (2), p.4015-4026

2015

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A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp

British journal of dermatology (1951), 2005-12, Vol.153 (6), p.1216-1219

2005

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Variants rs2758346, rs5746094, and rs2758331 of SOD2 gene: association study with breast cancer in a Mexican population and their analysis in silico

European review for medical and pharmacological sciences, 2024-02, Vol.28 (3), p.1163

2024

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Duplication 5q and Deletion 9p due to a t(5;9)(q34;p23) in 2 Cousins with Features of Hunter-McAlpine Syndrome and Hypothyroidism

Cytogenetic and genome research, 2011-02, Vol.132 (4), p.233-238

2011

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Autoantibodies to a miRNA-binding protein Argonaute2 (Su antigen) in patients with hepatitis C virus infection

Clinical and experimental rheumatology, 2010-11, Vol.28 (6), p.842

2010

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Wide clinical spectrum in Zimmermann-Laband syndrome

Genetic counseling, 2011, Vol.22 (1), p.1

2011

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Pulmonary function in ankylosing spondylitis: association with clinical variables

Rheumatology international, 2013-09, Vol.33 (9), p.2351-2358

2013

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Methylenetetrahydrofolate reductase C677T polymorphism and Factor V Leiden variant in Mexican women with preeclampsia/eclampsia

Blood cells, molecules, & diseases, 2005-07, Vol.35 (1), p.66-69

2005

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CHROMOSOMAL ABNORMALITIES IN PATIENTS WITH AZOOSPERMIA IN WESTERN MEXICO

Archives of andrology, 2006-03, Vol.52 (2), p.87-90

2006

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The ACTN3 R577X polymorphism is associated with inflammatory myopathies in a Mexican population

Scandinavian journal of rheumatology, 2012-10, Vol.41 (5), p.396-400

2012

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A variant example of familial Floating-Harbor syndrome?

Genetic counseling, 2003, Vol.14 (1), p.31

2003

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Floating-Harbor syndrome. A neuropsychological approach

Genetic counseling, 1996, Vol.7 (4), p.283

1996

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Guadalajara camptodactyly type III: a new probably autosomal dominant syndrome

Clinical dysmorphology, 2002-10, Vol.11 (4), p.243-247

2002

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A teenager with a t(X;17)(q22;q25) and ovarian failure

Genetic counseling, 2010-01, Vol.21 (3), p.269

2010

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Reproductive history in mothers of children with neural tube defects

Gynecologic and obstetric investigation, 2000-01, Vol.49 (4), p.255

2000

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Madelung's deformity from a rheumatologist's point of view

Rheumatology (Oxford, England), 1997-08, Vol.36 (8), p.925-926

1997

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Alphoidless centromere of a familial unstable inverted Y chromosome

Annales de génétique, 1996, Vol.39 (4), p.236

1996

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Zimmermann-Laband syndrome: further clinical delineation

Genetic counseling, 2005, Vol.16 (3), p.283

2005

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inv(9)(p24q13) in three sterile brothers

Annales de génétique, 2000, Vol.43 (1), p.51-54

2000

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GENE CORNER: A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp

British journal of dermatology (1951), 2005-12, Vol.153 (6), p.1216-1219

2005

Volltextzugriff (PDF)

Madelung's deformity from a rheumatologist's point of view

British journal of rheumatology, 1997-08, Vol.36 (8), p.925

1997

Volltextzugriff (PDF)

The ACTN3R577X polymorphism is associated with inflammatory myopathies in a Mexican population

Scandinavian journal of rheumatology, 2012, Vol.41 (5), p.396-400

2012

Volltextzugriff (PDF)

The C677T polymorphism of the methylenetetrahydrofolate reductase gene in Mexican mestizo neural-tube defect parents, control mestizo and native populations

Annales de génétique, 2000-04, Vol.43 (2), p.89-92

2000

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FISH characterisation of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation

American journal of medical genetics, 2001-11, Vol.103 (4), p.289-294

2001

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Polymorphisms C677T and A1298C in the MTHFR gene in Mexican patients with rheumatoid arthritis treated with methotrexate: implication with elevation of transaminases

Association of the C677T polymorphism in the methylenetetrahydrofolate reductase gene with breast cancer in a Mexican population

A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp

Variants rs2758346, rs5746094, and rs2758331 of SOD2 gene: association study with breast cancer in a Mexican population and their analysis in silico

Duplication 5q and Deletion 9p due to a t(5;9)(q34;p23) in 2 Cousins with Features of Hunter-McAlpine Syndrome and Hypothyroidism

Autoantibodies to a miRNA-binding protein Argonaute2 (Su antigen) in patients with hepatitis C virus infection

Wide clinical spectrum in Zimmermann-Laband syndrome

Pulmonary function in ankylosing spondylitis: association with clinical variables

Methylenetetrahydrofolate reductase C677T polymorphism and Factor V Leiden variant in Mexican women with preeclampsia/eclampsia

CHROMOSOMAL ABNORMALITIES IN PATIENTS WITH AZOOSPERMIA IN WESTERN MEXICO

The ACTN3 R577X polymorphism is associated with inflammatory myopathies in a Mexican population

A variant example of familial Floating-Harbor syndrome?

Floating-Harbor syndrome. A neuropsychological approach

Guadalajara camptodactyly type III: a new probably autosomal dominant syndrome

A teenager with a t(X;17)(q22;q25) and ovarian failure

Reproductive history in mothers of children with neural tube defects

Madelung's deformity from a rheumatologist's point of view

Alphoidless centromere of a familial unstable inverted Y chromosome

Zimmermann-Laband syndrome: further clinical delineation

inv(9)(p24q13) in three sterile brothers

GENE CORNER: A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp

Madelung's deformity from a rheumatologist's point of view

The ACTN3R577X polymorphism is associated with inflammatory myopathies in a Mexican population

The C677T polymorphism of the methylenetetrahydrofolate reductase gene in Mexican mestizo neural-tube defect parents, control mestizo and native populations

FISH characterisation of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation

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