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MARWAN SHINAWI, MD
MD
Clinical Genetics (M.D.) Physician
NPI: 1912087354IndividualAccepts Medicare
Specialties, Licenses & Credentials
Pediatrics Physician
Pediatrics
Code: 208000000X
2009029458(MO)
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
2009029458(MO)
CMS Specialties
PrimaryPEDIATRIC MEDICINE
Education
OTHER
Class of 1996
Research & Publications (20)
Syndromic thrombocytopenia and predisposition to acute myelogenous leukemia caused by constitutional microdeletions on chromosome 21q.
PMID 18487507·Blood·2008
8-other
Low-level mosaicism of trisomy 14: phenotypic and molecular characterization.
PMID 18412278·Am J Med Genet A·2008
5-case
Lymphedema of the lower extremity: is it genetic or nongenetic?
PMID 17641125·Clin Pediatr (Phila)·2007
5-case
Recognition of Smith-Lemli-Opitz syndrome (RSH) in the fetus: utility of ultrasonography and biochemical analysis in pregnancies with low maternal serum estriol.
PMID 16097001·Am J Med Genet A·2005
5-case
Extensive primary cutaneous herpes simplex virus type 1 infection in an infant following acute rotavirus gastroenteritis.
PMID 15717179·Eur J Pediatr·2005
5-case
Splicing mutation in the fibrillin-1 gene associated with neonatal Marfan syndrome and severe pulmonary emphysema with tracheobronchomalacia.
PMID 15666366·Pediatr Pulmonol·2005
5-case
Gastrointestinal tract cytomegalovirus infection with prolonged vomiting and fever in an immunocompetent child.
PMID 11519392·Isr Med Assoc J·2001
5-case
Mitochondrial neurogastrointestinal encephalopathy due to mutations in RRM2B.
PMID 19667227·Arch Neurol·2009
5-case
Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairment.
PMID 19584063·J Med Genet·2009
8-other
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response.
PMID 19525956·Nat Genet·2009
8-other
The MTHFR 677C-->T polymorphism and behaviors in children with autism: exploratory genotype-phenotype correlations.
PMID 19455642·Autism Res·2009
8-other
Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders.
PMID 19289393·J Med Genet·2009
8-other
Atypical presentation of VLCAD deficiency associated with a novel ACADVL splicing mutation.
PMID 19208414·Muscle Nerve·2009
5-case
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
PMID 19029900·Nat Genet·2008
8-other
15q13q14 deletions: phenotypic characterization and molecular delineation by comparative genomic hybridization.
PMID 18561338·Am J Med Genet A·2008
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
- 1 CHILDRENS PL, DIV PED GENETICS AND GENOMIC MED
SAINT LOUIS, MO 63110 - Phone
- (314) 454-6093
Quick Facts
- NPI
- 1912087354
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 30
- Publications
- 20
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