Detalhe da pesquisa
1.
Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1.
Clin Genet
; 98(4): 353-364, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33111345
2.
When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations.
Genet Med
; 20(1): 128-131, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28726807
3.
Chromosomal microarray findings in pregnancies with an isolated pelvic kidney.
J Perinat Med
; 47(1): 30-34, 2018 Dec 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-29813032
4.
The impact of third-trimester genetic counseling.
Arch Gynecol Obstet
; 297(3): 659-665, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29306968
5.
The association between maternal serum first trimester free ßhCG, second trimester intact hCG levels and foetal growth restriction and preeclampsia.
J Obstet Gynaecol
; 38(3): 363-366, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29385871
6.
The magnitude of elevated maternal serum human chorionic gonadotropin and pregnancy complications.
J Obstet Gynaecol
; 37(5): 576-579, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28604182
7.
Is the ratio of maternal serum to amniotic fluid AFP superior to serum levels as a predictor of pregnancy complications?
Arch Gynecol Obstet
; 293(4): 767-70, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26453361
8.
Telomere length and telomerase reverse transcriptase mRNA expression in patients with hepatitis C.
Hepatogastroenterology
; 60(127): 1713-6, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24634940
9.
Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome.
Nat Genet
; 32(3): 448-52, 2002 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-12389028
10.
Correlation between prenatal and postnatal penile and clitoral measurements.
J Clin Ultrasound
; 40(7): 394-8, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22733627
11.
Telomere aggregates in amniocytes with karyotype of balanced chromosomal rearrangements.
Hereditas
; 147(2): 90-3, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20536547
12.
Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1-8 does not cause Beals syndrome.
Eur J Med Genet
; 63(10): 104008, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32702406
13.
Maternal serum triple marker levels in immigrants to Israel from Ethiopia.
Fetal Diagn Ther
; 26(4): 200-2, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19940445
14.
Who should be offered fetal echocardiography? One center's experience with 3965 cases.
Isr Med Assoc J
; 11(9): 542-5, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19960848
15.
The yield of the prenatal work-up in intrauterine growth restriction and the spectrum of fetal abnormalities detected postnatally .
J Matern Fetal Neonatal Med
; 32(5): 753-759, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29020825
16.
Yemenite-Jewish families with Machado-Joseph disease (MJD/SCA3) share a recent common ancestor.
Eur J Hum Genet
; 27(11): 1731-1737, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31189928
17.
Non-visualization of fetal gallbladder in microarray era - a retrospective cohort study and review of the literature.
J Matern Fetal Neonatal Med
; 32(16): 2643-2648, 2019 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-29455582
18.
Four USH2A founder mutations underlie the majority of Usher syndrome type 2 cases among non-Ashkenazi Jews.
Genet Test
; 12(2): 289-94, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18452394
19.
Adverse outcome of pregnancies with extremely high levels of maternal serum human chorionic gonadotropin.
Fetal Diagn Ther
; 23(3): 233-6, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18417984
20.
The mid-gestation triple test profile among women diagnosed with vasa previa.
J Matern Fetal Neonatal Med
; 31(11): 1402-1406, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28385051