Variants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome

Anneke Kievit; F Tessadori; Hannie Douben; I Jordens; M Maurice; Jeannette Hoogeboom; R Hennekam; S Nampoothiri; H Kayserili; M Castori; M Whiteford; C Motter; C Melver; M Cunningham; A Hing; NM Kokitsu-Nakata; S Vendramini-Pittoli; A Richieri-Costa; AF Baas; CC Breugem; K Duran; M Massink; PWB Derksen; Wilfred van Ijcken; Leontine Unen; F Santos-Simarro; P Lapunzina; V Lopes; E Lustosa-Mendes; M Krall; A Slavotinek; V Martinez-Glez; J Bakkers; K L I van Gassen; Annelies de Klein; MJH van den Boogaard; G van Haaften

doi:10.1038/s41431-017-0010-5

Variants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome

Anneke Kievit, F Tessadori, Hannie Douben, I Jordens, M Maurice, Jeannette Hoogeboom, R Hennekam, S Nampoothiri, H Kayserili, M Castori, M Whiteford, C Motter, C Melver, M Cunningham, A Hing, NM Kokitsu-Nakata, S Vendramini-Pittoli, A Richieri-Costa, AF Baas, CC BreugemK Duran, M Massink, PWB Derksen, Wilfred van Ijcken, Leontine Unen, F Santos-Simarro, P Lapunzina, V Lopes, E Lustosa-Mendes, M Krall, A Slavotinek, V Martinez-Glez, J Bakkers, K L I van Gassen, Annelies de Klein, MJH van den Boogaard, G van Haaften

Clinical Genetics

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

16 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	210-219
Number of pages	10
Journal	European Journal of Human Genetics
Volume	26
Issue number	2
DOIs	https://doi.org/10.1038/s41431-017-0010-5
Publication status	Published - 2018

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10.1038/s41431-017-0010-5

http://hdl.handle.net/1765/104144

Cite this

Kievit, A., Tessadori, F., Douben, H., Jordens, I., Maurice, M., Hoogeboom, J., Hennekam, R., Nampoothiri, S., Kayserili, H., Castori, M., Whiteford, M., Motter, C., Melver, C., Cunningham, M., Hing, A., Kokitsu-Nakata, NM., Vendramini-Pittoli, S., Richieri-Costa, A., Baas, AF., ... van Haaften, G. (2018). Variants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome. European Journal of Human Genetics, 26(2), 210-219. https://doi.org/10.1038/s41431-017-0010-5

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title = "Variants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome",

author = "Anneke Kievit and F Tessadori and Hannie Douben and I Jordens and M Maurice and Jeannette Hoogeboom and R Hennekam and S Nampoothiri and H Kayserili and M Castori and M Whiteford and C Motter and C Melver and M Cunningham and A Hing and NM Kokitsu-Nakata and S Vendramini-Pittoli and A Richieri-Costa and AF Baas and CC Breugem and K Duran and M Massink and PWB Derksen and {van Ijcken}, Wilfred and Leontine Unen and F Santos-Simarro and P Lapunzina and V Lopes and E Lustosa-Mendes and M Krall and A Slavotinek and V Martinez-Glez and J Bakkers and {van Gassen}, {K L I} and {de Klein}, Annelies and {van den Boogaard}, MJH and {van Haaften}, G",

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doi = "10.1038/s41431-017-0010-5",

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Kievit, A, Tessadori, F, Douben, H, Jordens, I, Maurice, M, Hoogeboom, J, Hennekam, R, Nampoothiri, S, Kayserili, H, Castori, M, Whiteford, M, Motter, C, Melver, C, Cunningham, M, Hing, A, Kokitsu-Nakata, NM, Vendramini-Pittoli, S, Richieri-Costa, A, Baas, AF, Breugem, CC, Duran, K, Massink, M, Derksen, PWB, van Ijcken, W , Unen, L, Santos-Simarro, F, Lapunzina, P, Lopes, V, Lustosa-Mendes, E, Krall, M, Slavotinek, A, Martinez-Glez, V, Bakkers, J, van Gassen, KLI, de Klein, A, van den Boogaard, MJH & van Haaften, G 2018, 'Variants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome', European Journal of Human Genetics, vol. 26, no. 2, pp. 210-219. https://doi.org/10.1038/s41431-017-0010-5

TY - JOUR

T1 - Variants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome

AU - Kievit, Anneke

AU - Tessadori, F

AU - Douben, Hannie

AU - Jordens, I

AU - Maurice, M

AU - Hoogeboom, Jeannette

AU - Hennekam, R

AU - Nampoothiri, S

AU - Kayserili, H

AU - Castori, M

AU - Whiteford, M

AU - Motter, C

AU - Melver, C

AU - Cunningham, M

AU - Hing, A

AU - Kokitsu-Nakata, NM

AU - Vendramini-Pittoli, S

AU - Richieri-Costa, A

AU - Baas, AF

AU - Breugem, CC

AU - Duran, K

AU - Massink, M

AU - Derksen, PWB

AU - van Ijcken, Wilfred

AU - Unen, Leontine

AU - Santos-Simarro, F

AU - Lapunzina, P

AU - Lopes, V

AU - Lustosa-Mendes, E

AU - Krall, M

AU - Slavotinek, A

AU - Martinez-Glez, V

AU - Bakkers, J

AU - van Gassen, K L I

AU - de Klein, Annelies

AU - van den Boogaard, MJH

AU - van Haaften, G

PY - 2018

Y1 - 2018

U2 - 10.1038/s41431-017-0010-5

DO - 10.1038/s41431-017-0010-5

M3 - Article

VL - 26

SP - 210

EP - 219

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

SN - 1018-4813

IS - 2

ER -