Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Deborah Pergament"'
Autor:
Deborah Pergament, Katie Ilijic
Publikováno v:
Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 3, Iss 4, Pp 1437-1465 (2014)
Journal of Clinical Medicine, Vol 3, Iss 4, Pp 1437-1465 (2014)
This chapter is an overview of the current status of the law in the United States regarding prenatal genetic testing with an emphasis on issues related to professional liability and other challenges affecting patient access to prenatal genetic testin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6484c0ed569da6751e5fdf5e8ed8420d
https://doi.org/10.3390/jcm3041437
https://doi.org/10.3390/jcm3041437
Publikováno v:
Prenatal Diagnosis. 20:567-570
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::813b0fa2a835554d03c9849afd5880bb
https://doi.org/10.1002/1097-0223(200007)20:7<567::aid-pd877>3.0.co
https://doi.org/10.1002/1097-0223(200007)20:7<567::aid-pd877>3.0.co
Autor:
Deborah Pergament, Stéphane Viville
Publikováno v:
Prenatal Diagnosis. 18:1374-1380
Considerable differences in the regulatory oversight of preimplantation genetic diagnostic (PGD) services exist among countries, ranging from total bans on any embryo manipulation to the almost complete absence of any regulations or authority. A surv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8d413b1095d88c33f2f9f0b75e10d63
https://doi.org/10.1002/(sici)1097-0223(199812)18:13<1374::aid-pd492>3.0.co
https://doi.org/10.1002/(sici)1097-0223(199812)18:13<1374::aid-pd492>3.0.co
Autor:
Deborah, Pergament
Publikováno v:
Health matrix (Cleveland, Ohio : 1991). 23(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5b1349d77daf2ee813ad46ecbfd2f67b
https://pubmed.ncbi.nlm.nih.gov/23808099
https://pubmed.ncbi.nlm.nih.gov/23808099
Autor:
Deborah Pergament, Eugene Pergament
Publikováno v:
Best practiceresearch. Clinical obstetricsgynaecology. 26(5)
A broad range of testing modalities for fetal genetic disease has been established. These include carrier screening for single-gene mutations, first-trimester and second-trimester screening for chromosome abnormalities and open neural-tube defects, p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a088e40eefebb04f510f2b885ecb59b
https://pubmed.ncbi.nlm.nih.gov/22809468
https://pubmed.ncbi.nlm.nih.gov/22809468
Publikováno v:
Preimplantation Genetic Diagnosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67c3fb2882b3feb58fc05b944f574358
https://doi.org/10.1002/0470846615.ch13
https://doi.org/10.1002/0470846615.ch13
Publikováno v:
Prenatal diagnosis. 20(7)
Preimplantation genetic diagnosis (PGD) has not been performed in Germany. Existing German laws do not explicitly permit or prohibit PGD. German law does forbid the wasting of totipotent embryonic cells, fertilizing oocyctes without transferring them
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e856766e8f197b47202602c915962df
https://pubmed.ncbi.nlm.nih.gov/10913956
https://pubmed.ncbi.nlm.nih.gov/10913956