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MICHAEL MARBLE, MD

MD

Clinical Genetics (M.D.) Physician

NPI: 1699798603Individual

Specialties, Licenses & Credentials

Clinical Genetics (M.D.) PhysicianPrimary

Medical Genetics — Clinical Genetics (M.D.)

Code: 207SG0201X

10120R(LA)89-257(NM)
Clinical Biochemical Genetics Physician

Medical Genetics — Clinical Biochemical Genetics

Code: 207SG0202X

10120R(LA)
Pediatrics Physician

Pediatrics

Code: 208000000X

10120R(LA)

Research & Publications (10)

Neonatal vitamin B12 deficiency secondary to maternal subclinical pernicious anemia: identification by expanded newborn screening.
PMID 18410783·J Pediatr·2008
5-case
Living related liver transplant in a patient with argininosuccinic aciduria and cirrhosis: metabolic follow-up.
PMID 18367960·J Pediatr Gastroenterol Nutr·2008
5-case
Pelizaeus-Merzbacher syndrome: neurocognitive function in a family with carrier manifestations.
PMID 17568416·Am J Med Genet A·2007
5-case
Scalp defects, polythelia, microcephaly, and developmental delay: a new syndrome with apparent autosomal dominant inheritance.
PMID 11920840·Am J Med Genet·2002
5-case
45,X/47,XX,+18 and ring (18) mosaicism with mild phenotypic features including normal stature: clinical report and review of the literature.
PMID 19002012·Clin Dysmorphol·2009
5-case
Phenotypic features of a boy with trisomy of 16q22-->qter due to paternal Y; 16 translocation.
PMID 16155418·Clin Dysmorphol·2005
5-case
Trisomy 1q43 syndrome: a consistent phenotype with macrocephaly, characteristic face, developmental delay and cardiac anomalies.
PMID 15658621·Genet Couns·2004
5-case
Transposition of the great arteries and hypocalcemia in a patient with fetal hydantoin syndrome.
PMID 11840251·J Perinatol·2002
5-case
Home care & hospice's role in response to a bioterrorist event.
PMID 11813647·Caring·2002
8-other
Phenotypic features in a boy with monosomy 18 mosaicism.
PMID 11102928·Am J Med Genet·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
1699798603
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
4
Locations
1
Publications
10

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