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KWAME ANYANE-YEBOA, M.D.
M.D.
NPI: 1831190354Individual
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
130473-1(NY)
Research & Publications (14)
Changes in an inherited ring (22) due to meiotic recombination? Implications for genetic counseling.
PMID 19449399·Am J Med Genet A·2009
5-case
Incidence of aortic root dilatation in pectus excavatum and its association with Marfan syndrome.
PMID 18762608·Arch Pediatr Adolesc Med·2008
8-other
Neuropsychological characteristics of children with the 22q11 Deletion Syndrome: a descriptive analysis.
PMID 15823982·Child Neuropsychol·2005
8-other
Application of ROMA (representational oligonucleotide microarray analysis) to patients with cytogenetic rearrangements.
PMID 15714078·Genet Med·2005
5-case
Networks of attention in children with the 22q11 deletion syndrome.
PMID 15456687·Dev Neuropsychol·2004
4-observational
Congenital myopathy, recurrent secretory diarrhea, bullous eruption of skin, microcephaly, and deafness: a new genetic syndrome?
PMID 12476446·Am J Med Genet A·2003
5-case
Homozygosity for multiple contiguous single-nucleotide polymorphisms as an indicator of large heterozygous deletions: identification of a novel heterozygous 8-kb intragenic deletion (IVS7-19 to IVS15-17) in a patient with glycogen storage disease type II.
PMID 11854868·Am J Hum Genet·2002
8-other
Paternal germline mosaicism in Herlitz junctional epidermolysis bullosa.
PMID 12366701·Exp Dermatol·2002
5-case
Identification of six novel mutations in the acid alpha-glucosidase gene in three Spanish patients with infantile onset glycogen storage disease type II (Pompe disease).
PMID 11738358·Neuromuscul Disord·2002
5-case
First-trimester transvaginal ultrasonographic diagnosis of Dandy-Walker malformation.
PMID 11731890·Am J Perinatol·2001
5-case
Maternal germline mosaicism in dominant dystrophic epidermolysis bullosa.
PMID 11710955·J Invest Dermatol·2001
8-other
Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy.
PMID 11443545·Am J Hum Genet·2001
5-case
Nine novel mutations in NR0B1 (DAX1) causing adrenal hypoplasia congenita.
PMID 11748852·Hum Mutat·2001
8-other
Molecular mechanism for duplication 17p11.2- the homologous recombination reciprocal of the Smith-Magenis microdeletion.
PMID 10615134·Nat Genet·2000
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
- 1000 10TH AVE, SUITE 11A-GENETICS
NEW YORK, NY 10019 - Phone
- (212) 523-5895
Quick Facts
- NPI
- 1831190354
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 14
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