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YVES LACASSIE, MD

MD

Clinical Genetics (M.D.) Physician

NPI: 1558383570Individual

Specialties, Licenses & Credentials

Pediatrics Physician

Pediatrics

Code: 208000000X

013441(LA)
Clinical Genetics (M.D.) PhysicianPrimary

Medical Genetics — Clinical Genetics (M.D.)

Code: 207SG0201X

MD.013441(LA)

Research & Publications (12)

Provisional new syndrome of MR/MCA with evolving phenotype.
PMID 12407715·Am J Med Genet·2002
5-case
Array analysis and molecular studies of INI1 in an infant with deletion 22q13 (Phelan-McDermid syndrome) and atypical teratoid/rhabdoid tumor.
PMID 19334084·Am J Med Genet A·2009
5-case
Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11.
PMID 18565486·Am J Hum Genet·2008
8-other
Is trisomy 14 mosaic a clinically recognizable syndrome?--case report and review.
PMID 18449929·Am J Med Genet A·2008
5-case
An unusual presentation of trisomy 13.
PMID 18438899·Am J Med Genet A·2008
5-case
Adams-Oliver syndrome in siblings with central nervous system findings, epilepsy, and developmental delay: refining the features of a severe autosomal recessive variant.
PMID 18203152·Am J Med Genet A·2008
5-case
17beta-hydroxysteroid dehydrogenase 3 deficiency in a male pseudohermaphrodite.
PMID 17509588·Fertil Steril·2008
5-case
Mosaic trisomy 22: report of a patient with normal intelligence.
PMID 15551336·Am J Med Genet A·2005
5-case
Congenital glaucoma and neurofibromatosis in a monozygotic twin: case report and review of the literature.
PMID 12940659·J Child Neurol·2003
5-case
De novo paracentric inversion (X)(q26q28) with features mimicking Prader-Willi syndrome.
PMID 12900904·Am J Med Genet A·2003
5-case
Provisionally unique autosomal recessive syndrome due to significant consanguinity.
PMID 11503158·Am J Med Genet·2001
5-case
Syndrome of microcephaly, mental retardation, and tracheoesophageal fistula associated with features of Rett syndrome.
PMID 10641614·J Child Neurol·2000
5-case

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

Contact & Hours

Address
CHILDREN'S HOSPITAL - GENETICS, 200 HENRY CLAY AVENUE
NEW ORLEANS, LA 70118

Location

Practice Location

CHILDREN'S HOSPITAL - GENETICS, NEW ORLEANS, LA
(504) 896-9254

Quick Facts

NPI
1558383570
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
2
Locations
1
Publications
12

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