Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Gita Tan-Sindhunata"'
Autor:
Yil Severijns, Hein de Vries, Gita Tan-Sindhunata, Kyra Stuurman, Cecile Ottenheim, Klaske Lichtenbelt, Sander van Kuijk, Sara Joosten, Elisa J. F. Houwink, Rik Crutzen, Nicole Corsten-Janssen, Emilia Bijlsma, Christine de Die-Smulders, Liesbeth van Osch
Publikováno v:
Health Psychology Bulletin; Vol 7 (2023); 17–26
Introduction: Couples at high risk of transmitting a genetic disease to their offspring have several reproductive options. As decision making is often experienced as difficult, there is a need for a decision aid (DA), to assist couples in their repro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cee5936365139e4f3cc1243b6606ee0
https://doi.org/10.5334/hpb.39
https://doi.org/10.5334/hpb.39
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 157(38)
When two successive pregnancies end in intra-uterine fetal death (IUFD), the question of whether it is coincidental or if there is an underlying abnormality arises. Although diagnostic investigations into the underlying cause are not always carried o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::eb0b50624c129ffb9a2befbd5a20c238
https://pubmed.ncbi.nlm.nih.gov/24330791
https://pubmed.ncbi.nlm.nih.gov/24330791
Autor:
Gita Tan-Sindhunata, Charles H.C.M. Buys, Aravinda Chakravarti, Robert M. W. Hofstra, Carel Meijers, Rein P. Stulp, Jan Osinga, Ying Wu, Erik J. Kamsteeg, Misha Angrist, Conny M.A. van Ravenswaaij-Arts, Danielle Majoor-Krakauer
Publikováno v:
Nature Genetics, 12, pp. 445-447
Nature Genetics, 12(4), 445-447. Nature Publishing Group
Nature Genetics, 12, 4, pp. 445-447
Nature Genetics, 12, 445-447
Hofstra, R M W, Osinga, J, Tan-Sindhunata, G, Wu, Y, Kamsteeg, E J, Stulp, R P, Van Ravenswaaij-Arts, C, Majoor-Krakauer, D, Angrist, M, Chakravarti, A, Meijers, C & Buys, C H C M 1996, ' A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome) ', Nature Genetics, vol. 12, no. 4, pp. 445-447 . https://doi.org/10.1038/ng0496-445
Nature Genetics, 12(4), 445-447. Nature Publishing Group
Nature Genetics, 12, 4, pp. 445-447
Nature Genetics, 12, 445-447
Hofstra, R M W, Osinga, J, Tan-Sindhunata, G, Wu, Y, Kamsteeg, E J, Stulp, R P, Van Ravenswaaij-Arts, C, Majoor-Krakauer, D, Angrist, M, Chakravarti, A, Meijers, C & Buys, C H C M 1996, ' A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome) ', Nature Genetics, vol. 12, no. 4, pp. 445-447 . https://doi.org/10.1038/ng0496-445
Hirschsprung disease (HSCR) or colonic aganglionosis is a congenital disorder characterized by an absence of intramural ganglia along variable lengths of the colon resulting in intestinal obstruction. The incidence of HSCR is 1 in 5,000 live births.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::470367cbde44beed553638dee1f9530d
https://hdl.handle.net/2066/23620
https://hdl.handle.net/2066/23620