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1.
Community data-driven approach to identify pathogenic founder variants for pan-ethnic carrier screening panels.
Hum Genomics
; 17(1): 30, 2023 03 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-36978159
2.
[THE RISK FOR CLINICALLY SIGNIFICANT COPY NUMBER VARIANTS IN PREGNANCIES WITH TWO SOFT MARKERS].
Harefuah
; 163(6): 365-368, 2024 Jun.
Artículo
en Hebreo
| MEDLINE | ID: mdl-38884289
3.
Lessons learned from the first national population-based genetic carrier-screening program for Duchenne muscular dystrophy.
Genet Med
; 25(12): 100981, 2023 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-37712502
4.
[MOH SCREENING FOR TBCD IN COCHIN JEWS: COLLABORATION BETWEEN MEDICAL, RESEARCH AND COMMUNITY MEMBERS IN ACHIEVING PUBLIC HEALTH GOALS].
Harefuah
; 162(6): 359-361, 2023 Jun.
Artículo
en Hebreo
| MEDLINE | ID: mdl-37394437
5.
[SUMMARY AND UPDATES IN THE FIELD OF GENETIC TESTING IN ISRAEL - AS OF 2022].
Harefuah
; 162(6): 386-392, 2023 Jun.
Artículo
en Hebreo
| MEDLINE | ID: mdl-37394443
6.
Colchicine treatment increases the risk for fetal chromosomal aberrations-an observational study and systematic literature review.
Rheumatology (Oxford)
; 60(5): 2342-2347, 2021 05 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-33179053
7.
Population-based screening for breast and ovarian cancer risk due to BRCA1 and BRCA2.
Proc Natl Acad Sci U S A
; 111(39): 14205-10, 2014 Sep 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-25192939
8.
Factors that affect the decision to undergo amniocentesis in women with normal Down syndrome screening results: it is all about the age.
Health Expect
; 18(6): 2306-17, 2015 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-24816429
9.
A Priori Attitudes Predict Amniocentesis Uptake in Women of Advanced Maternal Age: A Pilot Study.
J Health Commun
; 20(9): 1107-13, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26065331
10.
BRCA genetic testing of individuals from families with low prevalence of cancer: experiences of carriers and implications for population screening.
Genet Med
; 14(7): 688-94, 2012 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-22481128
11.
A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies.
Sci Rep
; 11(1): 19099, 2021 09 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-34580403
12.
Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic Anomalies.
Obstet Gynecol
; 132(6): 1368-1375, 2018 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-30399107
13.
The limited effect of information on Israeli pregnant women at advanced maternal age who decide to undergo amniocentesis.
Isr J Health Policy Res
; 4: 23, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26284151
14.
The best marker combination using the integrated screening test approach for detecting various chromosomal aneuploidies.
J Perinat Med
; 33(5): 392-8, 2005.
Artículo
en Inglés
| MEDLINE | ID: mdl-16238533
15.
Are amniotic fluid alpha-fetoprotein levels influenced by the gender in twin pairs?
Fetal Diagn Ther
; 18(4): 281-3, 2003.
Artículo
en Inglés
| MEDLINE | ID: mdl-12835590
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