Decision‐making for non‐invasive prenatal testing for Down syndrome: Hong Kong Chinese women's preferences for individual vs relational autonomy (English)
- New search for: Lau, J.Y.C.
- New search for: Yi, H.
- New search for: Ahmed, S.
- New search for: Lau, J.Y.C.
- New search for: Yi, H.
- New search for: Ahmed, S.
In:
Clinical Genetics
;
89
, 5
;
550-556
;
2016
- Article (Journal) / Electronic Resource
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Title:Decision‐making for non‐invasive prenatal testing for Down syndrome: Hong Kong Chinese women's preferences for individual vs relational autonomy
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Contributors:
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Published in:Clinical Genetics ; 89, 5 ; 550-556
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Publisher:
- New search for: Blackwell Publishing Ltd
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Publication date:2016-05-01
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Size:7 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Keywords:
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Source:
Table of contents – Volume 89, Issue 5
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 521
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Issue Information ‐ Editorial Board| 2016
- 523
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Clinical implementation of NIPT – technical and biological challengesBrady, P. / Brison, N. / Van Den Bogaert, K. / de Ravel, T. / Peeters, H. / Van Esch, H. / Devriendt, K. / Legius, E. / Vermeesch, J.R. et al. | 2016
- 531
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Genomic futures of prenatal screening: ethical reflectionDondorp, W.J. / Page‐Christiaens, G.C.M.L. / de Wert, G.M.W.R et al. | 2016
- 539
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Refining the continuum of CFTR‐associated disorders in the era of newborn screeningLevy, H. / Nugent, M. / Schneck, K. / Stachiw‐Hietpas, D. / Laxova, A. / Lakser, O. / Rock, M. / Dahmer, M.K. / Biller, J. / Nasr, S.Z. et al. | 2016
- 550
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Decision‐making for non‐invasive prenatal testing for Down syndrome: Hong Kong Chinese women's preferences for individual vs relational autonomyLau, J.Y.C. / Yi, H. / Ahmed, S. et al. | 2016
- 557
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Recognition of the Cornelia de Lange syndrome phenotype with facial dysmorphology novel analysisBasel‐Vanagaite, L. / Wolf, L. / Orin, M. / Larizza, L. / Gervasini, C. / Krantz, I.D. / Deardoff, M.A. et al. | 2016
- 564
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Expanding the clinical spectrum of the ‘HDAC8‐phenotype’ – implications for molecular diagnostics, counseling and risk predictionParenti, I. / Gervasini, C. / Pozojevic, J. / Wendt, K.S. / Watrin, E. / Azzollini, J. / Braunholz, D. / Buiting, K. / Cereda, A. / Engels, H. et al. | 2016
- 574
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Wide allelic heterogeneity with predominance of large IDS gene complex rearrangements in a sample of Mexican patients with Hunter syndromeAlcántara‐Ortigoza, M.A. / García‐de Teresa, B. / González‐del Angel, A. / Berumen, J. / Guardado‐Estrada, M. / Fernández‐Hernández, L. / Navarrete‐Martínez, J.I. / Maza‐Morales, M. / Rius‐Domínguez, R. et al. | 2016
- 584
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A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndromeNizon, M. / Henry, M. / Michot, C. / Baumann, C. / Bazin, A. / Bessières, B. / Blesson, S. / Cordier‐Alex, M.‐P. / David, A. / Delahaye‐Duriez, A. et al. | 2016
- 590
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Mutations in WNT9B are associated with Mayer–Rokitansky–Küster–Hauser syndromeWaschk, D.E.J. / Tewes, A.‐C. / Römer, T. / Hucke, J. / Kapczuk, K. / Schippert, C. / Hillemanns, P. / Wieacker, P. / Ledig, S. et al. | 2016
- 597
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Association analysis between HFM1 variation and primary ovarian insufficiency in Chinese womenPu, D. / Wang, C. / Cao, J. / Shen, Y. / Jiang, H. / Liu, J. / Wu, B.L. / Zhang, W. / Wu, J. et al. | 2016
- 603
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A non‐sense MCM9 mutation in a familial case of primary ovarian insufficiencyFauchereau, F. / Shalev, S. / Chervinsky, E. / Beck‐Fruchter, R. / Legois, B. / Fellous, M. / Caburet, S. / Veitia, R.A. et al. | 2016
- 608
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NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiencyBouali, N. / Francou, B. / Bouligand, J. / Lakhal, B. / Malek, I. / Kammoun, M. / Warszawski, J. / Mougou, S. / Saad, A. / Guiochon‐Mantel, A. et al. | 2016
- 614
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Risk assessment of medically assisted reproduction and advanced maternal ages in the development of Prader–Willi syndrome due to UPD(15)matMatsubara, K. / Murakami, N. / Fukami, M. / Kagami, M. / Nagai, T. / Ogata, T. et al. | 2016
- 620
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First‐trimester spontaneous pregnancy loss – molecular analysis using multiplex ligation‐dependent probe amplificationZimowski, J. G. / Massalska, D. / Pawelec, M. / Bijok, J. / Michałowska, A. / Roszkowski, T. et al. | 2016
- 625
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Early growth and development impairments in patients with ganglioside GM3 synthase deficiencyWang, H. / Wang, A. / Wang, D. / Bright, A. / Sency, V. / Zhou, A. / Xin, B. et al. | 2016
- 630
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Genetic counselling difficulties and ethical implications of incidental findings from array‐CGH: a 7‐year national surveyLefebvre, M. / Sanlaville, D. / Marle, N. / Thauvin‐Robinet, C. / Gautier, E. / Chehadeh, S.E. / Mosca‐Boidron, A.‐L. / Thevenon, J. / Edery, P. / Alex‐Cordier, M.‐P. et al. | 2016
- 636
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Corrigendum| 2016
- e1
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Homozygous FIBP nonsense variant responsible of syndromic overgrowth, with overgrowth, macrocephaly, retinal coloboma and learning disabilitiesThauvin‐Robinet, C. / Duplomb‐Jego, L. / Limoge, F. / Picot, D. / Masurel, A. / Terriat, B. / Champilou, C. / Minot, D. / St‐Onge, J. / Kuentz, P. et al. | 2016