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KAREN GRIPP, MD

MD

Clinical Genetics (M.D.) Physician

NPI: 1790877678Individual

Specialties, Licenses & Credentials

Clinical Genetics (M.D.) PhysicianPrimary

Medical Genetics — Clinical Genetics (M.D.)

Code: 207SG0201X

C10006183(DE)

Research & Publications (20)

Significant overlap and possible identity of macrocephaly capillary malformation and megalencephaly polymicrogyria-polydactyly hydrocephalus syndromes.
PMID 19353582·Am J Med Genet A·2009
5-case
Expanding the phenotype of SPONASTRIME dysplasia to include short dental roots, hypogammaglobulinemia, and cataracts.
PMID 18203204·Am J Med Genet A·2008
5-case
Costello syndrome associated with novel germline HRAS mutations: an attenuated phenotype?
PMID 18247425·Am J Med Genet A·2008
5-case
Further delineation of the phenotype resulting from BRAF or MEK1 germline mutations helps differentiate cardio-facio-cutaneous syndrome from Costello syndrome.
PMID 17551924·Am J Med Genet A·2007
8-other
Somatic mosaicism for an HRAS mutation causes Costello syndrome.
PMID 16969868·Am J Med Genet A·2006
8-other
HRAS mutation analysis in Costello syndrome: genotype and phenotype correlation.
PMID 16329078·Am J Med Genet A·2006
8-other
Elevated catecholamine metabolites in patients with Costello syndrome.
PMID 15211656·Am J Med Genet A·2004
5-case
22q11.2 deletion syndrome and selective IgM deficiency: an association of a common chromosomal abnormality with a rare immunodeficiency.
PMID 15103727·Am J Med Genet A·2004
8-other
Five additional Costello syndrome patients with rhabdomyosarcoma: proposal for a tumor screening protocol.
PMID 11857556·Am J Med Genet·2002
8-other
Tumor predisposition in Costello syndrome.
PMID 16010679·Am J Med Genet C Semin Med Genet·2005
6-review
Bilateral microtia and cleft palate in cousins with Diamond-Blackfan anemia.
PMID 11424144·Am J Med Genet·2001
5-case
Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination.
PMID 10835638·Nat Genet·2000
7-preclinical
Mutations in the human TWIST gene.
PMID 10649491·Hum Mutat·2000
6-review
Male-to-male transmission of Costello syndrome: G12S HRAS germline mutation inherited from a father with somatic mosaicism.
PMID 19206176·Am J Med Genet A·2009
8-other
Preaxial hallucal polydactyly as a marker for diabetic embryopathy.
PMID 18798547·Birth Defects Res A Clin Mol Teratol·2009
8-other
Prenatal features of Costello syndrome: ultrasonographic findings and atrial tachycardia.
PMID 19382114·Prenat Diagn·2009
5-case
The diagnosis of Costello syndrome: nomenclature in Ras/MAPK pathway disorders.
PMID 18386799·Am J Med Genet A·2008
4-observational
Clarification of previously reported Costello syndrome patients.
PMID 18302240·Am J Med Genet A·2008
8-other
Molecular aspects, clinical aspects and possible treatment modalities for Costello syndrome: Proceedings from the 1st International Costello Syndrome Research Symposium 2007.
PMID 18412122·Am J Med Genet A·2008
8-other
Costello syndrome and related disorders.
PMID 18025929·Curr Opin Pediatr·2007
8-other

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

Contact & Hours

Address
A.I. DUPONT HOSPITAL FOR CHILDREN, 1600 ROCKLAND ROAD
WILMINGTON, DE 19803

Location

Practice Location

A.I. DUPONT HOSPITAL FOR CHILDREN, WILMINGTON, DE
(302) 651-4000

Quick Facts

NPI
1790877678
Entity Type
Individual
Gender
Female
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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