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Retraso global del desarrollo y microcefalia posnatal: síndrome de Bainbridge-Ropers con una nueva variante de novo en ASXL3

Neurología (Barcelona, Spain), 2018-09, Vol.33 (7), p.484-486

2018

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Frequency of the thermolabile variant C677T in the MTHFR gene and lack of association with neural tube defects in the State of Yucatan, Mexico

Clinical genetics, 2002-11, Vol.62 (5), p.394-398

2002

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Forensic potential of the STR DXYS156 in Mexican populations: inference of X-linked allele null

Legal medicine (Tokyo, Japan), 2006, Vol.8 (1), p.52-54

2006

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Identifying deletions in the dystrophin gene and detecting carriers in families with Duchenne's/Becker's muscular dystrophy

Revista de neurologiá, 2009-01, Vol.48 (2), p.66-70

2009

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Global developmental delay and postnatal microcephaly: Bainbridge-Ropers syndrome with a new mutation in ASXL3

Neurología (Barcelona, English ed. ), 2018-09, Vol.33 (7), p.484-486

2018

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Identificación de deleciones en el gen de la distrofina y detección de portadoras en familias con distrofia muscular de Duchenne/Becker

Revista de neurologiá, 2009, Vol.48 (2), p.66

2009

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High prevalence of 5G allele in Amerindian tribes and Mestizos from Mexico at 4G/5G PAI-I gene promoter polymorphism

Thrombosis and haemostasis, 2005-05, Vol.93 (5), p.1005

2005

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Paraoxonase 1 (PON1) polymorphisms and haplotypes as risk factors for having Spina bifida-affected offspring in southeast Mexico

Toxicology letters, 2010-07, Vol.196, p.S45-S46

2010

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ANÁLISIS DE POLIMORFISMOS EN EL GEN SLC22A1 EN UNA POBLACIÓN DE YUCATÁN, MÉXICO

Revista clínica de la escuela de medicina UCR-HSJD, 2013-12, Vol.3 (10)

2013

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Chromosomic findings in patients with paroxysmal nocturnal hemoglobinuria

International journal of hematology, 1993-10, Vol.58 (3), p.163-167

1993

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Espectro de malformaciones congénitas observadas en recién nacidos de progenitores consanguíneos

Anales de pediatría (Barcelona, Spain : 2003), 2006, Vol.64 (1), p.5-10

2006

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Spectrum of congenital malformations observed in neonates of consanguineous parents

Anales de pediatría (Barcelona, Spain : 2003), 2006-01, Vol.64 (1), p.5-10

2006

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TAR-like syndrome in a consanguineous Mayan girl

American journal of medical genetics, 1992-07, Vol.43 (5), p.805-807

1992

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Identical twins with the classical form of Schwartz-Jampel syndrome

Clinical dysmorphology, 1997-01, Vol.6 (1), p.45-50

1997

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Addendum to “Forensic potential of the STR DXYS156 in Mexican populations: Inference of X-linked allele null”: [Legal Med 8 (2006) 52–54]

Legal medicine (Tokyo, Japan), 2006-05, Vol.8 (3), p.201-202

2006

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Announcement of Population Data: Forensic potential of the STR DXYS156 in Mexican populations: inference of X-linked allele null

Legal medicine (Tokyo, Japan), 2006-01, Vol.8 (1), p.52-54

2006

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Global developmental delay and postnatal microcephaly: Bainbridge-Ropers syndrome with a new mutation in ASXL3

Neurologia (Barcelona, Spain), 2018, Vol.33 (7), p.484-486

2018

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A new case of Klippel-Trenaunay-Weber (KTW) syndrome: Evidence of autosomal dominant inheritance

American journal of medical genetics, 1996-06, Vol.63 (3), p.426-427

1996

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Full mosaic monosomy 22 in a child with DiGeorge syndrome facial appearance

American journal of medical genetics, 1998-03, Vol.76 (2), p.150-153

1998

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Cytogenetic research in couples with recurrent spontaneous gestational losses

Ginecologia y obstetricia de Mexico, 1996-11, Vol.64, p.503

1996

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Nocturnal paroxysmal hemoglobinuria: analysis of 36 cases

Sangre (Zaragoza), 1987, Vol.32 (1), p.27

1987

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Retraso global del desarrollo y microcefalia posnatal: síndrome de Bainbridge-Ropers con una nueva variante de novo en ASXL3

Frequency of the thermolabile variant C677T in the MTHFR gene and lack of association with neural tube defects in the State of Yucatan, Mexico

Forensic potential of the STR DXYS156 in Mexican populations: inference of X-linked allele null

Identifying deletions in the dystrophin gene and detecting carriers in families with Duchenne's/Becker's muscular dystrophy

Global developmental delay and postnatal microcephaly: Bainbridge-Ropers syndrome with a new mutation in ASXL3

Identificación de deleciones en el gen de la distrofina y detección de portadoras en familias con distrofia muscular de Duchenne/Becker

High prevalence of 5G allele in Amerindian tribes and Mestizos from Mexico at 4G/5G PAI-I gene promoter polymorphism

Paraoxonase 1 (PON1) polymorphisms and haplotypes as risk factors for having Spina bifida-affected offspring in southeast Mexico

ANÁLISIS DE POLIMORFISMOS EN EL GEN SLC22A1 EN UNA POBLACIÓN DE YUCATÁN, MÉXICO

Chromosomic findings in patients with paroxysmal nocturnal hemoglobinuria

Espectro de malformaciones congénitas observadas en recién nacidos de progenitores consanguíneos

Spectrum of congenital malformations observed in neonates of consanguineous parents

TAR-like syndrome in a consanguineous Mayan girl

Identical twins with the classical form of Schwartz-Jampel syndrome

Addendum to “Forensic potential of the STR DXYS156 in Mexican populations: Inference of X-linked allele null”: [Legal Med 8 (2006) 52–54]

Announcement of Population Data: Forensic potential of the STR DXYS156 in Mexican populations: inference of X-linked allele null

Global developmental delay and postnatal microcephaly: Bainbridge-Ropers syndrome with a new mutation in ASXL3

A new case of Klippel-Trenaunay-Weber (KTW) syndrome: Evidence of autosomal dominant inheritance

Full mosaic monosomy 22 in a child with DiGeorge syndrome facial appearance

Cytogenetic research in couples with recurrent spontaneous gestational losses

Nocturnal paroxysmal hemoglobinuria: analysis of 36 cases

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