2nd-trimester maternal serum human chorionic gonadotropin and α-fetoprotein levels in male and female fetuses with Down syndromeLEHAVI, Ofer; AIZENSTEIN, Orna; EVANS, Mark I et al.Fetal diagnosis and therapy. 2005, Vol 20, Num 3, pp 235-238, issn 1015-3837, 4 p.Article

Rapid prenatal diagnosis of aneuploidy for chromosomes 21, 18, 13, and X by quantitative fluorescence polymerase chain reactionOCHSHORN, Yifat; BAR-SHIRA, Anat; JONISH, Anat et al.Fetal diagnosis and therapy. 2006, Vol 21, Num 4, pp 326-331, issn 1015-3837, 6 p.Article

First-trimester nuchal translucency and maternal serum free β-hCG and PAPP-A can detect triploidy and determine the parental originYARON, Yuval; OCHSHORN, Yifat; TSABARI, Sigal et al.Prenatal diagnosis. 2004, Vol 24, Num 6, pp 445-450, issn 0197-3851, 6 p.Article

Clinical evaluation of isolated nonvisualized fetal gallbladderOCHSHORN, Yifat; ROSNER, Guy; BAREL, Dalit et al.Prenatal diagnosis. 2007, Vol 27, Num 8, pp 699-703, issn 0197-3851, 5 p.Article

Nomograms for the sonographic measurement of the Fetal philtrum and ChinGULL, Ilan; WOLMAN, Igal; MERLOB, Paul et al.Fetal diagnosis and therapy. 2005, Vol 20, Num 2, pp 127-131, issn 1015-3837, 5 p.Article

The mitochondrial DNA mutation (ΔmtDNA⁵²⁸⁶) in human oocytes: Correlation with age and IVF outcomesYESODI, Vered; YARON, Yuval; LESSING, Joseph B et al.Journal of assisted reproduction and genetics. 2002, Vol 19, Num 2, pp 60-66, issn 1058-0468Article

ScreeningEVANS, Mark I; KRIVCHENIA, Eric L; YARON, Yuval et al.Baillière's best practice & research. Clinical obstetrics & gynaecology. 2002, Vol 16, Num 5, pp 645-657, issn 1521-6934, 13 p.Article

High prevalence of the prothrombin gene mutation in women with intrauterine growth retardation, abruptio placentae and second trimester lossKUPFERMINC, Michael J; PERI, Hava; ZWANG, Eti et al.Acta obstetricia et gynecologica Scandinavica. 2000, Vol 79, Num 11, pp 963-967, issn 0001-6349Article

Effect of fetal gender on first trimester markers and on Down syndrome screeningYARON, Yuval; WOLMAN, Igal; KUPFERMINC, Michael J et al.Prenatal diagnosis. 2001, Vol 21, Num 12, pp 1027-1030, issn 0197-3851Article

Second-trimester maternal serum alpha-fetoprotein (MSAFP) is elevated in women with adverse pregnancy outcome associated with inherited thrombophiliasOCHSHORN, Yifat; KUPFERMINC, Michael J; ELDOR, Amiram et al.Prenatal diagnosis. 2001, Vol 21, Num 8, pp 658-661, issn 0197-3851Article

Preimplantation genetic diagnosis of canavan diseaseYARON, Yuval; SCHWARTZ, Tamar; MEY-RAZ, Nava et al.Fetal diagnosis and therapy. 2005, Vol 20, Num 5, pp 465-468, issn 1015-3837, 4 p.Article

Brachydactyly A-1 mutations restricted to the central region of the N-terminal active fragment of Indian HedgehogBYRNES, Ashley M; RACACHO, Lemuel; BULMAN, Dennis E et al.European journal of human genetics. 2009, Vol 17, Num 9, pp 1112-1120, issn 1018-4813, 9 p.Article

Loeys-Dietz Syndrome in Pregnancy: A Case Description and Report of a Novel MutationGUTMAN, Guy; BARIS, Hagit N; HIRSCH, Raphael et al.Fetal diagnosis and therapy. 2009, Vol 26, Num 1, pp 35-37, issn 1015-3837, 3 p.Article

Preimplantation genetic diagnosis for fragile X syndrome : is there increased transmission of abnormal FMR1 alleles among female heterozygotes?RECHES, Adi; MALCOV, Mira; BEN-YOSEF, Dalit et al.Prenatal diagnosis. 2009, Vol 29, Num 1, pp 57-61, issn 0197-3851, 5 p.Conference Paper

Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restrictionDE CRESCENZO, Agostina; SPARAGO, Angela; CERRATO, Flavia et al.Journal of medical genetics. 2013, Vol 50, Num 2, pp 99-103, issn 0022-2593, 5 p.Article

Preimplantation genetic diagnosis (PGD) for duchenne muscular dystrophy (DMD) by triplex-nested PCRMALCOV, Mira; BEN-YOSEF, Dalit; SCHWARTZ, Tamar et al.Prenatal diagnosis. 2005, Vol 25, Num 13, pp 1200-1205, issn 0197-3851, 6 p.Article

Maternal serum HCG is higher in the presence of a female fetus as early as week 3 post-fertilizationYARON, Yuval; LEHAVI, Ofer; ORR-URTREGER, Avi et al.Human reproduction (Oxford. Print). 2002, Vol 17, Num 2, pp 485-489, issn 0268-1161Article

First trimester PAPP-A in the detection of non-Down syndrome aneuploidyOCHSHORN, Yifat; KUPFERMINC, Michael J; WOLMAN, Igal et al.Prenatal diagnosis. 2001, Vol 21, Num 7, pp 547-549, issn 0197-3851Article

Aneuploidy screening: a position statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, January 2011BENN, Peter; BORRELL, Antoni; SPENCER, Kevin et al.Prenatal diagnosis. 2011, Vol 31, Num 6, pp 519-522, issn 0197-3851, 4 p.Article

Insight into the intrinsic sensitivity of the PCR assay used to detect CMV infection in amniotic fluid specimensAVIDOR, Boaz; EFRAT, Gabi; BERGER, Stephen A et al.Journal of clinical virology. 2004, Vol 29, Num 4, pp 260-270, issn 1386-6532, 11 p.Article

A novel founder mutation in the RNASEL gene, 471deIAAAG, is associated with prostate Cancer in Ashkenazi jewsRENNERT, Hanna; BERCOVICH, Dani; KADOURI, Luna et al.American journal of human genetics. 2002, Vol 71, Num 4, pp 981-984, issn 0002-9297, 4 p.Article

Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromesVALENTE, Enza Maria; LOGAN, Clare V; ADAMS, Matthew et al.Nature genetics. 2010, Vol 42, Num 7, pp 619-625, issn 1061-4036, 7 p.Article

Multiple genes in human 20q13 chromosomal region are involved in an advanced prostate cancer xenograftBAR-SHIRA, Anat; PINTHUS, Jehonathan H; ROZOVSKY, Uri et al.Cancer research (Baltimore). 2002, Vol 62, Num 23, pp 6803-6807, issn 0008-5472, 5 p.Article