Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis

K Buiting; B Dittrich; S Gross; C Lich; C Färber; T Buchholz; E Smith; A Reis; J Bürger; MM Nöthen; U Barth-Witte; B Janssen; D Abeliovich; I Lerer; Ans van den Ouweland; Dicky Halley; C Schrander-Stumpel; H Smeets; P Meinecke; S Malcolm; A Gardner; M Lalande; RD Nicholls; K Friend; A Schulze; G Matthijs; H Kokkonen; P Hilbert; L van Maldergem; G Glover; P Carbonell; P Willems; G Gillessen-Kaesbach; B Horsthemke

doi:10.1086/301935

Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis

K Buiting, B Dittrich, S Gross, C Lich, C Färber, T Buchholz, E Smith, A Reis, J Bürger, MM Nöthen, U Barth-Witte, B Janssen, D Abeliovich, I Lerer, Ans van den Ouweland, Dicky Halley, C Schrander-Stumpel, H Smeets, P Meinecke, S MalcolmA Gardner, M Lalande, RD Nicholls, K Friend, A Schulze, G Matthijs, H Kokkonen, P Hilbert, L van Maldergem, G Glover, P Carbonell, P Willems, G Gillessen-Kaesbach, B Horsthemke

Clinical Genetics

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

134 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	170-180
Number of pages	11
Journal	American Journal of Human Genetics
Volume	63
DOIs	https://doi.org/10.1086/301935
Publication status	Published - 1998

Research programs

EMC MGC-02-96-01

Access to Document

10.1086/301935

http://hdl.handle.net/1765/57733

Cite this

Buiting, K., Dittrich, B., Gross, S., Lich, C., Färber, C., Buchholz, T., Smith, E., Reis, A., Bürger, J., Nöthen, MM., Barth-Witte, U., Janssen, B., Abeliovich, D., Lerer, I., van den Ouweland, A., Halley, D., Schrander-Stumpel, C., Smeets, H., Meinecke, P., ... Horsthemke, B. (1998). Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis. American Journal of Human Genetics, 63, 170-180. https://doi.org/10.1086/301935

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author = "K Buiting and B Dittrich and S Gross and C Lich and C F{\"a}rber and T Buchholz and E Smith and A Reis and J B{\"u}rger and MM N{\"o}then and U Barth-Witte and B Janssen and D Abeliovich and I Lerer and {van den Ouweland}, Ans and Dicky Halley and C Schrander-Stumpel and H Smeets and P Meinecke and S Malcolm and A Gardner and M Lalande and RD Nicholls and K Friend and A Schulze and G Matthijs and H Kokkonen and P Hilbert and {van Maldergem}, L and G Glover and P Carbonell and P Willems and G Gillessen-Kaesbach and B Horsthemke",

year = "1998",

doi = "10.1086/301935",

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pages = "170--180",

journal = "American Journal of Human Genetics",

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Buiting, K, Dittrich, B, Gross, S, Lich, C, Färber, C, Buchholz, T, Smith, E, Reis, A, Bürger, J, Nöthen, MM, Barth-Witte, U, Janssen, B, Abeliovich, D, Lerer, I, van den Ouweland, A, Halley, D, Schrander-Stumpel, C, Smeets, H, Meinecke, P, Malcolm, S, Gardner, A, Lalande, M, Nicholls, RD, Friend, K, Schulze, A, Matthijs, G, Kokkonen, H, Hilbert, P, van Maldergem, L, Glover, G, Carbonell, P, Willems, P, Gillessen-Kaesbach, G & Horsthemke, B 1998, 'Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis', American Journal of Human Genetics, vol. 63, pp. 170-180. https://doi.org/10.1086/301935

TY - JOUR

T1 - Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis

AU - Buiting, K

AU - Dittrich, B

AU - Gross, S

AU - Lich, C

AU - Färber, C

AU - Buchholz, T

AU - Smith, E

AU - Reis, A

AU - Bürger, J

AU - Nöthen, MM

AU - Barth-Witte, U

AU - Janssen, B

AU - Abeliovich, D

AU - Lerer, I

AU - van den Ouweland, Ans

AU - Halley, Dicky

AU - Schrander-Stumpel, C

AU - Smeets, H

AU - Meinecke, P

AU - Malcolm, S

AU - Gardner, A

AU - Lalande, M

AU - Nicholls, RD

AU - Friend, K

AU - Schulze, A

AU - Matthijs, G

AU - Kokkonen, H

AU - Hilbert, P

AU - van Maldergem, L

AU - Glover, G

AU - Carbonell, P

AU - Willems, P

AU - Gillessen-Kaesbach, G

AU - Horsthemke, B

PY - 1998

Y1 - 1998

U2 - 10.1086/301935

DO - 10.1086/301935

M3 - Article

SN - 0002-9297

VL - 63

SP - 170

EP - 180

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

ER -