Back to Search
YIFAH YARON, MD
MD
Internal Medicine Physician
NPI: 1255582169Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
A87573(CA)
Research & Publications (20)
Preimplantation aneuploid embryos undergo self-correction in correlation with their developmental potential.
PMID 18829021·Fertil Steril·2009
8-other
Detection of spinal muscular atrophy carriers by nested polymerase chain reaction of single sperm cells.
PMID 16544998·Genet Test·2006
8-other
First-trimester nuchal translucency and maternal serum free beta-hCG and PAPP-A can detect triploidy and determine the parental origin.
PMID 15229844·Prenat Diagn·2004
8-other
The clinical application of spectral karyotyping (SKY) in the analysis of prenatally diagnosed extra structurally abnormal chromosomes (ESACs).
PMID 12533818·Prenat Diagn·2003
5-case
MECP2 mutations in Israel: implications for molecular analysis, genetic counseling, and prenatal diagnosis in Rett syndrome.
PMID 12325033·Hum Mutat·2002
8-other
Decreased first trimester PAPP-A is a predictor of adverse pregnancy outcome.
PMID 12224070·Prenat Diagn·2002
8-other
Maternal serum HCG is higher in the presence of a female fetus as early as week 3 post-fertilization.
PMID 11821300·Hum Reprod·2002
8-other
Effect of fetal gender on first trimester markers and on Down syndrome screening.
PMID 11746159·Prenat Diagn·2001
8-other
Identification of novel functional regions important for the activity of HOXB7 in mammalian cells.
PMID 11290787·J Immunol·2001
7-preclinical
Elucidation of abnormal fertilization by single-cell analysis with fluorescence in situ hybridization and polymorphic marker analysis.
PMID 19110241·Fertil Steril·2009
5-case
Dynamic modification strategy of the Israeli carrier screening protocol: inclusion of the Oriental Jewish Group to the cystic fibrosis panel.
PMID 19265749·Genet Med·2009
8-other
Preimplantation genetic diagnosis for fragile X syndrome: is there increased transmission of abnormal FMR1 alleles among female heterozygotes?
PMID 19097038·Prenat Diagn·2009
8-other
Current controversies in prenatal diagnosis 3: For prenatal diagnosis, should we offer less or more than metaphase karyotyping?
PMID 19012273·Prenat Diagn·2009
8-other
Brachydactyly A-1 mutations restricted to the central region of the N-terminal active fragment of Indian Hedgehog.
PMID 19277064·Eur J Hum Genet·2009
8-other
Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literature.
PMID 19006240·Hum Mutat·2009
6-review
Elucidating the origin of chromosomal aberrations in IVF embryos by preimplantation genetic analysis.
PMID 18177997·Mol Cell Endocrinol·2008
6-review
Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoform.
PMID 18949062·Mol Vis·2008
7-preclinical
Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryos.
PMID 18371394·Cell Stem Cell·2007
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1510 4TH ST STE 1
BERKELEY, CA 94710 - Phone
- (510) 525-8980
Quick Facts
- NPI
- 1255582169
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile