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DOROTHY GRANGE, MD

MD

Clinical Genetics (M.D.) Physician

NPI: 1801812128IndividualAccepts Medicare

Specialties, Licenses & Credentials

Clinical Biochemical Genetics Physician

Medical Genetics — Clinical Biochemical Genetics

Code: 207SG0202X

R9J19(MO)
Pediatrics Physician

Pediatrics

Code: 208000000X

R9J19(MO)
Clinical Genetics (M.D.) PhysicianPrimary

Medical Genetics — Clinical Genetics (M.D.)

Code: 207SG0201X

R9J19(MO)

CMS Specialties

PrimaryMEDICAL GENETICS AND GENOMICS

Additional

PEDIATRIC MEDICINE

Education

UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE

Class of 1981

Research & Publications (20)

CHILD syndrome caused by deficiency of 3beta-hydroxysteroid-delta8, delta7-isomerase.
PMID 10710233·Am J Med Genet·2000
5-case
Efficacy of sapropterin dihydrochloride in increasing phenylalanine tolerance in children with phenylketonuria: a phase III, randomized, double-blind, placebo-controlled study.
PMID 19261295·J Pediatr·2009
3-trial
Response monitoring in children with phenylketonuria.
PMID 19210041·Neuropsychology·2009
8-other
Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genes.
PMID 19188198·J Med Genet·2009
5-case
Pilocytic astrocytoma in a child with Noonan syndrome.
PMID 19621452·Pediatr Blood Cancer·2009
5-case
Mutations in the GGCX and ABCC6 genes in a family with pseudoxanthoma elasticum-like phenotypes.
PMID 18800149·J Invest Dermatol·2009
5-case
Case report: Congenital knee dislocation in a patient with larsen syndrome and a novel filamin B mutation.
PMID 18322662·Clin Orthop Relat Res·2008
5-case
Two new patients with Curry-Jones syndrome with trichoblastoma and medulloblastoma suggest an etiologic role of the sonic hedgehog-patched-GLI pathway.
PMID 18798318·Am J Med Genet A·2008
5-case
Zero Liquid Discharge approach in plating industry: treatment of degreasing effluents by electrocoagulation and anodic oxidation.
PMID 18725717·Water Sci Technol·2008
8-other
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
PMID 19029900·Nat Genet·2008
8-other

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

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Contact & Hours

Address
1 CHILDRENS PL, DIV PED GENETICS AND GENOMIC MED
SAINT LOUIS, MO 63110

Quick Facts

NPI
1801812128
Entity Type
Individual
Gender
Female
Medicare
Accepted
Specialties
3
Locations
1
Years in Practice
45
Publications
20

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