Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe

D Wellesley; Helen Dolk; PA Boyd; M Haeusler; V Nelen; E Garne; B Khoshnood; B Doray; A Rissmann; C Mullaney; E Calzolari; M Bakker; J Salvador; M-C Addor; E Draper; J Rankin; D Tucker

doi:10.1038/ejhg.2011.246

Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe

D Wellesley
, Helen Dolk
, PA Boyd
, M Haeusler
, V Nelen
, E Garne
, B Khoshnood
, B Doray
, A Rissmann
, C Mullaney
, E Calzolari
, M Bakker
, J Salvador
, M-C Addor
, E Draper
, J Rankin
, D Tucker

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	521-526
Journal	European Journal of Human Genetics
Volume	20
Issue number	5
DOIs	https://doi.org/10.1038/ejhg.2011.246
Publication status	Published (in print/issue) - 2012

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

Access to Document

10.1038/ejhg.2011.246

Cite this

Wellesley, D., Dolk, H., Boyd, PA., Haeusler, M., Nelen, V., Garne, E., Khoshnood, B., Doray, B., Rissmann, A., Mullaney, C., Calzolari, E., Bakker, M., Salvador, J., Addor, M.-C., Draper, E., Rankin, J., & Tucker, D. (2012). Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe. European Journal of Human Genetics, 20(5), 521-526. https://doi.org/10.1038/ejhg.2011.246

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author = "D Wellesley and Helen Dolk and PA Boyd and M Haeusler and V Nelen and E Garne and B Khoshnood and B Doray and A Rissmann and C Mullaney and E Calzolari and M Bakker and J Salvador and M-C Addor and E Draper and J Rankin and D Tucker",

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Wellesley, D, Dolk, H, Boyd, PA, Haeusler, M, Nelen, V, Garne, E, Khoshnood, B, Doray, B, Rissmann, A, Mullaney, C, Calzolari, E, Bakker, M, Salvador, J, Addor, M-C, Draper, E, Rankin, J & Tucker, D 2012, 'Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe', European Journal of Human Genetics, vol. 20, no. 5, pp. 521-526. https://doi.org/10.1038/ejhg.2011.246

TY - JOUR

T1 - Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe

AU - Wellesley, D

AU - Dolk, Helen

AU - Boyd, PA

AU - Haeusler, M

AU - Nelen, V

AU - Garne, E

AU - Khoshnood, B

AU - Doray, B

AU - Rissmann, A

AU - Mullaney, C

AU - Calzolari, E

AU - Bakker, M

AU - Salvador, J

AU - Addor, M-C

AU - Draper, E

AU - Rankin, J

AU - Tucker, D

PY - 2012

Y1 - 2012

U2 - 10.1038/ejhg.2011.246

DO - 10.1038/ejhg.2011.246

M3 - Article

SN - 1476-5438

VL - 20

SP - 521

EP - 526

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 5

ER -