Detalhe da pesquisa
1.
[ADJUSTING THE DAYS OF BLEEDING AND PURITY FOR A BRIDE BEFORE THE WEDDING. THE RELIGIOUS FEMALE GYNECOLOGISTS CONFERENCE WAS HELD ON THE 15TH OF JULY 2021 IN JERUSALEM, AND AN ONLINE UPDATE CONFERENCE WAS HELD ON NOVEMBER 5TH 2022].
Harefuah
; 163(1): 54-56, 2024 Jan.
Artigo
em Hebraico
| MEDLINE | ID: mdl-38297422
2.
[DECISION-MAKING FACILITATION MODEL IN UNCERTAINTY - GENETIC COUNSELING FOR PATHOGENIC AMNIOCENTESIS CMA RESULTS].
Harefuah
; 162(9): 581-586, 2023 Nov.
Artigo
em Hebraico
| MEDLINE | ID: mdl-37965854
3.
Residual risk for clinically significant copy number variants in low-risk pregnancies, following exclusion of noninvasive prenatal screening-detectable findings.
Am J Obstet Gynecol
; 226(4): 562.e1-562.e8, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34762861
4.
Biallelic truncating variants in the muscular A-type lamin-interacting protein (MLIP) gene cause myopathy with hyperCKemia.
Eur J Neurol
; 29(4): 1174-1180, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34935254
5.
Prenatal and postnatal chromosomal microarray analysis in 885 cases of various congenital heart defects.
Arch Gynecol Obstet
; 306(4): 1007-1013, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35083553
6.
Teaching clinicians practical genomic medicine: 7 years' experience in a tertiary care center.
Genet Med
; 22(10): 1703-1709, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32616942
7.
Induction of labor versus expectant management after successful external cephalic version.
Birth
; 46(4): 623-627, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31612564
8.
Prevalence of high-penetrant copy number variants in 7734 low-risk pregnancies.
Am J Obstet Gynecol MFM
; 5(12): 101201, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37871696
9.
Chromosomal Microarray Analysis Compared With Noninvasive Prenatal Testing in Pregnancies With Abnormal Maternal Serum Screening.
Obstet Gynecol
; 139(5): 877-887, 2022 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35576346
10.
Vici syndrome in Israel: Clinical and molecular insights.
Front Genet
; 13: 991721, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36204321