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IAN KRANTZ, M.D.
M.D.
NPI: 1306860325IndividualAccepts Medicare
Specialties, Licenses & Credentials
Medical Genetics — Clinical Cytogenetics
Code: 207SC0300X
MD052766L(PA)
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
MD052766L(PA)
CMS Specialties
PrimaryMEDICAL GENETICS AND GENOMICS
Education
OTHER
Class of 1991
Research & Publications (20)
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B.
PMID 15146186·Nat Genet·2004
4-observational
Exclusion of linkage to the CDL1 gene region on chromosome 3q26.3 in some familial cases of Cornelia de Lange syndrome.
PMID 11391654·Am J Med Genet·2001
8-other
Screening for postpartum depression with the Edinburgh Postnatal Depression Scale (EPDS): an ethical analysis.
PMID 18519287·Scand J Public Health·2008
8-other
FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation.
PMID 19668217·Nat Genet·2009
8-other
Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA.
PMID 18996922·Hum Mol Genet·2009
8-other
SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variation.
PMID 19058200·Hum Mutat·2009
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
- 3401 CIVIC CENTER BLVD
PHILADELPHIA, PA 19104 - Phone
- (215) 590-2920
Quick Facts
- NPI
- 1306860325
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 1
- Years in Practice
- 35
- Publications
- 20
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