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IGNATIA VAN DEN VEYVER, MD

MD

Maternal & Fetal Medicine Physician

NPI: 1962582205Individual

Specialties, Licenses & Credentials

Clinical Genetics (M.D.) Physician

Medical Genetics — Clinical Genetics (M.D.)

Code: 207SG0201X

J6785(TX)
Maternal & Fetal Medicine PhysicianPrimary

Obstetrics & Gynecology — Maternal & Fetal Medicine

Code: 207VM0101X

J6785(TX)

Research & Publications (20)

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases.
PMID 19012303·Prenat Diagn·2009
8-other
Comparative genomic hybridization and prenatal diagnosis.
PMID 16601480·Curr Opin Obstet Gynecol·2006
6-review
Presence of filamin in the astrocytic inclusions of Aicardi syndrome.
PMID 14738943·Pediatr Neurol·2004
5-case
Microphthalmia with linear skin defects (MLS), Aicardi, and Goltz syndromes: are they related X-linked dominant male-lethal disorders?
PMID 12900577·Cytogenet Genome Res·2002
7-preclinical
Genetic basis of Rett syndrome.
PMID 12112732·Ment Retard Dev Disabil Res Rev·2002
6-review
Genetic effects of methylation diets.
PMID 12055346·Annu Rev Nutr·2002
6-review
Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome.
PMID 11738862·Brain Dev·2001
6-review
Skewed X inactivation in X-linked disorders.
PMID 11480916·Semin Reprod Med·2001
6-review
Methyl-CpG-binding protein 2 mutations in Rett syndrome.
PMID 10826991·Curr Opin Genet Dev·2000
6-review
Non-random X chromosome inactivation in Aicardi syndrome.
PMID 19116729·Hum Genet·2009
8-other
Neuroimaging aspects of Aicardi syndrome.
PMID 18925666·Am J Med Genet A·2008
8-other
A recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles.
PMID 18039680·Mol Hum Reprod·2008
8-other
Phenotype and management of Aicardi syndrome: new findings from a survey of 69 children.
PMID 17621479·J Child Neurol·2007
8-other
Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia.
PMID 17546030·Nat Genet·2007
8-other
Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization.
PMID 17108764·Genet Med·2006
4-observational
Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients.
PMID 16859563·BMC Med Genet·2006
7-preclinical
Newborn screening and prenatal diagnosis for Rett syndrome: implications for therapy.
PMID 16225835·J Child Neurol·2005
6-review
Facial and physical features of Aicardi syndrome: infants to teenagers.
PMID 16158440·Am J Med Genet A·2005
8-other
Tooth enamel defects in mice with a deletion at the Arhgap 6/Amel X locus.
PMID 16007484·Calcif Tissue Int·2005
7-preclinical
Recurrent biparental hydatidiform mole: additional evidence for a 1.1-Mb locus in 19q13.4 and candidate gene analysis.
PMID 15979551·J Soc Gynecol Investig·2005
8-other

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Via practice · 2 locations total

Address
1504 TAUB LOOP
HOUSTON, TX 77030

Locations (2)

Practice Location

1504 TAUB LOOP, HOUSTON, TX
(713) 526-4243

Practice Location

6620 MAIN ST, HOUSTON, TX
(713) 798-7500

Quick Facts

NPI
1962582205
Entity Type
Individual
Gender
Female
Medicare
Not confirmed
Specialties
2
Locations
2
Publications
20

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