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DEBORAH KRAKOW MD
MD
Clinical Genetics (M.D.) Physician
NPI: 1689657579IndividualAccepts Medicare
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
G57061(CA)
Obstetrics & Gynecology Physician
Obstetrics & Gynecology
Code: 207V00000X
G57061(CA)
Maternal & Fetal Medicine Physician
Obstetrics & Gynecology — Maternal & Fetal Medicine
Code: 207VM0101X
G57061(CA)
Orthopaedic Surgery Physician
Orthopaedic Surgery
Code: 207X00000X
G57061(CA)
Education
OTHER
Class of 1984
Research & Publications (20)
Guidelines for the prenatal diagnosis of fetal skeletal dysplasias.
PMID 19265753·Genet Med·2009
7-preclinical
Mutations in the gene encoding the calcium-permeable ion channel TRPV4 produce spondylometaphyseal dysplasia, Kozlowski type and metatropic dysplasia.
PMID 19232556·Am J Hum Genet·2009
8-other
Evaluation of prenatal-onset osteochondrodysplasias by ultrasonography: a retrospective and prospective analysis.
PMID 18627037·Am J Med Genet A·2008
8-other
Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis.
PMID 14991055·Nat Genet·2004
8-other
Analysis of clones from a human cartilage cDNA library provides insight into chondrocyte gene expression and identifies novel candidate genes for the osteochondrodysplasias.
PMID 12765844·Mol Genet Metab·2003
8-other
Use of three-dimensional ultrasound imaging in the diagnosis of prenatal-onset skeletal dysplasias.
PMID 12768559·Ultrasound Obstet Gynecol·2003
8-other
Use of three-dimensional ultrasonography in differentiating craniosynostosis from severe fetal molding.
PMID 11316322·J Ultrasound Med·2001
5-case
Identification of human FEM1A, the ortholog of a C. elegans sex-differentiation gene.
PMID 11733146·Gene·2001
4-observational
Exclusion of the Ellis-van Creveld region on chromosome 4p16 in some families with asphyxiating thoracic dystrophy and short-rib polydactyly syndromes.
PMID 10951528·Eur J Hum Genet·2000
8-other
Ciliary abnormalities due to defects in the retrograde transport protein DYNC2H1 in short-rib polydactyly syndrome.
PMID 19361615·Am J Hum Genet·2009
8-other
The Erlenmeyer flask bone deformity in the skeletal dysplasias.
PMID 19444897·Am J Med Genet A·2009
6-review
Prenatal diagnosis of Larsen syndrome caused by a mutation in the filamin B gene.
PMID 19085972·Prenat Diagn·2009
5-case
A recessive skeletal dysplasia, SEMD aggrecan type, results from a missense mutation affecting the C-type lectin domain of aggrecan.
PMID 19110214·Am J Hum Genet·2009
8-other
Expanded clinical spectrum of spondylocarpotarsal synostosis syndrome and possible manifestation in a heterozygous father.
PMID 18257094·Am J Med Genet A·2008
5-case
Spondylocarpotarsal synostosis: long-term follow-up of a case due to FLNB mutations.
PMID 18386804·Am J Med Genet A·2008
5-case
Disruption of the Flnb gene in mice phenocopies the human disease spondylocarpotarsal synostosis syndrome.
PMID 17635842·Hum Mol Genet·2008
7-preclinical
Sprouty 2 disturbs FGFR3 degradation in thanatophoric dysplasia type II: a severe form of human achondroplasia.
PMID 18485666·Cell Signal·2008
7-preclinical
ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-beta bioavailability regulation.
PMID 18677313·Nat Genet·2008
8-other
Angulated femurs and the skeletal dysplasias: experience of the International Skeletal Dysplasia Registry (1988-2006).
PMID 17486589·Am J Med Genet A·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
Via practice · 4 locations total
- Address
- 200 UCLA MEDICAL PLZ STE 430
LOS ANGELES, CA 90095 - Phone
- (310) 794-7274
Locations (4)
Quick Facts
- NPI
- 1689657579
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 4
- Locations
- 4
- Years in Practice
- 42
- Publications
- 20
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