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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
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
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
Characterization of de novo microdeletions involving 17q11.2q12 identified through chromosomal comparative genomic hybridization.
PMID 17916097·Clin Genet·2007
5-case
The response of patients with phenylketonuria and elevated serum phenylalanine to treatment with oral sapropterin dihydrochloride (6R-tetrahydrobiopterin): a phase II, multicentre, open-label, screening study.
PMID 17846916·J Inherit Metab Dis·2007
3-trial
Increased progerin expression associated with unusual LMNA mutations causes severe progeroid syndromes.
PMID 17469202·Hum Mutat·2007
5-case
Cantu syndrome in a woman and her two daughters: Further confirmation of autosomal dominant inheritance and review of the cardiac manifestations.
PMID 16835932·Am J Med Genet A·2006
5-case
New cases of Bohring-Opitz syndrome, update, and critical review of the literature.
PMID 16691589·Am J Med Genet A·2006
5-case
Severe bilateral panlobular emphysema and pulmonary arterial hypoplasia: unusual manifestations of Menkes disease.
PMID 16278898·Am J Med Genet A·2005
5-case
Trisomy 20q13 --> 20qter in a girl with multiple congenital malformations and a recombinant chromosome 20 inherited from a paternal inversion (20)(p13q13.1): clinical report and review of the trisomy 20q phenotype.
PMID 16092120·Am J Med Genet A·2005
5-case
A previously unidentified amino-terminal domain regulates transcriptional activity of wild-type and disease-associated human GLI2.
PMID 15994174·Hum Mol Genet·2005
7-preclinical
Sialidosis presenting as severe nonimmune fetal hydrops is associated with two novel mutations in lysosomal alpha-neuraminidase.
PMID 15908988·J Perinatol·2005
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
- 1801812128
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 1
- Years in Practice
- 45
- Publications
- 20
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