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ANNE SLAVOTINEK, M.D.
M.D.
NPI: 1649212994IndividualAccepts Medicare
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
A79866(CA)35.145121(OH)
CMS Specialties
PrimaryPEDIATRIC MEDICINE
Education
OTHER
Class of 1987
Research & Publications (20)
Novel FGFR2 deletion in a patient with Beare-Stevenson-like syndrome.
PMID 19610084·Am J Med Genet A·2009
5-case
Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome.
PMID 19447831·J Med Genet·2009
8-other
Sequence variants in the HLX gene at chromosome 1q41-1q42 in patients with diaphragmatic hernia.
PMID 19459883·Clin Genet·2009
7-preclinical
Two novel STRA6 mutations in a patient with anophthalmia and diaphragmatic eventration.
PMID 19213032·Am J Med Genet A·2009
5-case
Congenital diaphragmatic hernia and microtia in a newborn with mycophenolate mofetil (MMF) exposure: phenocopy for Fryns syndrome or broad spectrum of teratogenic effects?
PMID 19449404·Am J Med Genet A·2009
5-case
Clinical and molecular studies of patients with characteristics of Opitz G/BBB syndrome shows a novel MID1 mutation.
PMID 18697196·Am J Med Genet A·2008
8-other
Phenotypic variation in trismus-pseudocamptodactyly syndrome caused by a recurrent MYH8 mutation.
PMID 18049072·Clin Dysmorphol·2008
8-other
Novel microdeletion syndromes detected by chromosome microarrays.
PMID 18512078·Hum Genet·2008
6-review
Candidate genes for congenital diaphragmatic hernia from animal models: sequencing of FOG2 and PDGFRalpha reveals rare variants in diaphragmatic hernia patients.
PMID 17568391·Eur J Hum Genet·2007
7-preclinical
Agenesis of the corpus callosum, optic coloboma, intractable seizures, craniofacial and skeletal dysmorphisms: an autosomal recessive disorder similar to Temtamy syndrome.
PMID 17632789·Am J Med Genet A·2007
5-case
Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes.
PMID 17655765·BMC Med Genet·2007
5-case
Oculo-ectodermal syndrome: is arachnoid cyst a common finding?
PMID 17159512·Clin Dysmorphol·2007
6-review
Cleft lip with or without cleft palate: frequency in different ethnic populations from the UCSF craniofacial clinic.
PMID 17726687·Am J Med Genet A·2007
8-other
Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination.
PMID 17517692·Hum Mol Genet·2007
7-preclinical
Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation.
PMID 17273977·Am J Hum Genet·2007
8-other
Manitoba Oculotrichoanal (MOTA) syndrome: report of eight new cases.
PMID 17352387·Am J Med Genet A·2007
5-case
Single gene disorders associated with congenital diaphragmatic hernia.
PMID 17436300·Am J Med Genet C Semin Med Genet·2007
7-preclinical
KBG syndrome: report of twins, neurological characteristics, and delineation of diagnostic criteria.
PMID 17230487·Am J Med Genet A·2007
5-case
Subtypes of frontonasal dysplasia are useful in determining clinical prognosis.
PMID 17955515·Am J Med Genet A·2007
5-case
Population-based analysis of left- and right-sided diaphragmatic hernias demonstrates different frequencies of selected additional anomalies.
PMID 18008313·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 · 2 locations total
- Address
- 3333 BURNET AVE., ML 4006
CINCINNATI, OH 45229 - Phone
- (513) 636-4760
Quick Facts
- NPI
- 1649212994
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 2
- Years in Practice
- 39
- Publications
- 20
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