Found: 11
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Motives and considerations regarding PGT in couples carrying a structural chromosomal abnormality: a qualitative exploration.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 7, p. 1719, doi. 10.1007/s10815-020-01810-w
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- Article
Preimplantation genetic testing for more than one genetic condition: clinical and ethical considerations and dilemmas.
- Published in:
- 2019
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- Publication type:
- journal article
The cognitive and socio-emotional development of 5-year-old children born after PGD.
- Published in:
- 2018
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- Publication type:
- journal article
Reproductive Decision Support: Preferences and Needs of Couples at Risk for Hereditary Cancer and Clinical Geneticists.
- Published in:
- Journal of Genetic Counseling, 2018, v. 27, n. 4, p. 920, doi. 10.1007/s10897-017-0204-6
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- Article
Support needs of couples with hereditary breast and ovarian cancer during reproductive decision making.
- Published in:
- 2018
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- Publication type:
- journal article
Awareness and attitude regarding reproductive options of persons carrying a BRCA mutation and their partners.
- Published in:
- 2017
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- Publication type:
- journal article
Recurrent miscarriage in translocation carriers: no differences in clinical characteristics between couples who accept and couples who decline PGD.
- Published in:
- Human Reproduction, 2015, v. 30, n. 2, p. 484, doi. 10.1093/humrep/deu314
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- Publication type:
- Article
Decision-making on preimplantation genetic diagnosis and prenatal diagnosis: a challenge for couples with hereditary breast and ovarian cancer.
- Published in:
- 2014
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- Publication type:
- Journal Article
Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012.
- Published in:
- 2013
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- Publication type:
- journal article
Anencephaly in monozygotic twins and recurrence risk.
- Published in:
- Prenatal Diagnosis, 1998, v. 18, n. 8, p. 867, doi. 10.1002/(SICI)1097-0223(199808)18:8<867::AID-PD1366>3.0.CO;2-E
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- Publication type:
- Article
Severe feeding problems and congenital laryngostenosis in a patient with 3q23 deletion.
- Published in:
- European Journal of Pediatrics, 1997, v. 156, n. 8, p. 636, doi. 10.1007/s004310050681
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- Article