CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental Delays.

Christian Windpassinger; J Piard; C Bonnard; M Alfadhel; S Lim; X Bisteau; S Blouin; NB Ali; AYJ Ng; H Lu; S Tohari; SZA Talib; N van Hul; MJ Caldez; L Van Maldergem; G Yigit; H Kayserili; SA Youssef; V Coppola; A de Bruin; L Tessarollo; H Choi; Verena Rupp; K Roetzer; P Roschger; K Klaushofer; J Altmüller; S Roy; B Venkatesh; R Ganger; F Grill; F Ben Chehida; B Wollnik; U Altunoglu; A Al Kaissi; B Reversade; P Kaldis

doi:10.1016/j.ajhg.2017.08.003

CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental Delays.

Christian Windpassinger (Erstautor*in)
, J Piard
, C Bonnard
, M Alfadhel
, S Lim
, X Bisteau
, S Blouin
, NB Ali
, AYJ Ng
, H Lu
, S Tohari
, SZA Talib
, N van Hul
, MJ Caldez
, L Van Maldergem
, G Yigit
, H Kayserili
, SA Youssef
, V Coppola
, A de Bruin

L Tessarollo, H Choi, Verena Rupp, K Roetzer, P Roschger, K Klaushofer, J Altmüller, S Roy, B Venkatesh, R Ganger, F Grill, F Ben Chehida, B Wollnik, U Altunoglu, A Al Kaissi, B Reversade, P Kaldis

Diagnostik- & Forschungsinstitut für Humangenetik

Publikation: Beitrag in Fachzeitschrift › Originalarbeit

34 Quellenangaben (Web of Science)

Originalsprache	Englisch
Fachzeitschrift	American Journal of Human Genetics
DOIs	https://doi.org/10.1016/j.ajhg.2017.08.003
Publikationsstatus	Veröffentlicht - 2017

Wissenschaftszweige

301 Medizinisch-theoretische Wissenschaften, Pharmazie
305 Andere Humanmedizin, Gesundheitswissenschaften

Forschungsfelder

Neurowissenschaften

Zugriff auf Dokument

10.1016/j.ajhg.2017.08.003

Andere Dateien und Links

Dieses zitieren

Windpassinger, C., Piard, J., Bonnard, C., Alfadhel, M., Lim, S., Bisteau, X., Blouin, S., Ali, NB., Ng, AYJ., Lu, H., Tohari, S., Talib, SZA., van Hul, N., Caldez, MJ., Van Maldergem, L., Yigit, G., Kayserili, H., Youssef, SA., Coppola, V., ... Kaldis, P. (2017). CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental Delays. American Journal of Human Genetics. https://doi.org/10.1016/j.ajhg.2017.08.003

@article{9d58c47e2a4240d685c8bcbfafa10425,

title = "CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental Delays.",

author = "Christian Windpassinger and J Piard and C Bonnard and M Alfadhel and S Lim and X Bisteau and S Blouin and NB Ali and AYJ Ng and H Lu and S Tohari and SZA Talib and \{van Hul\}, N and MJ Caldez and \{Van Maldergem\}, L and G Yigit and H Kayserili and SA Youssef and V Coppola and \{de Bruin\}, A and L Tessarollo and H Choi and Verena Rupp and K Roetzer and P Roschger and K Klaushofer and J Altm{\"u}ller and S Roy and B Venkatesh and R Ganger and F Grill and \{Ben Chehida\}, F and B Wollnik and U Altunoglu and \{Al Kaissi\}, A and B Reversade and P Kaldis",

year = "2017",

doi = "10.1016/j.ajhg.2017.08.003",

language = "English",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

}

Windpassinger, C, Piard, J, Bonnard, C, Alfadhel, M, Lim, S, Bisteau, X, Blouin, S, Ali, NB, Ng, AYJ, Lu, H, Tohari, S, Talib, SZA, van Hul, N, Caldez, MJ, Van Maldergem, L, Yigit, G, Kayserili, H, Youssef, SA, Coppola, V, de Bruin, A, Tessarollo, L, Choi, H, Rupp, V, Roetzer, K, Roschger, P, Klaushofer, K, Altmüller, J, Roy, S, Venkatesh, B, Ganger, R, Grill, F, Ben Chehida, F, Wollnik, B, Altunoglu, U, Al Kaissi, A, Reversade, B & Kaldis, P 2017, 'CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental Delays.', American Journal of Human Genetics. https://doi.org/10.1016/j.ajhg.2017.08.003

TY - JOUR

T1 - CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental Delays.

AU - Piard, J

AU - Bonnard, C

AU - Alfadhel, M

AU - Lim, S

AU - Bisteau, X

AU - Blouin, S

AU - Ali, NB

AU - Ng, AYJ

AU - Lu, H

AU - Tohari, S

AU - Talib, SZA

AU - van Hul, N

AU - Caldez, MJ

AU - Van Maldergem, L

AU - Yigit, G

AU - Kayserili, H

AU - Youssef, SA

AU - Coppola, V

AU - de Bruin, A

AU - Tessarollo, L

AU - Choi, H

AU - Rupp, Verena

AU - Roetzer, K

AU - Roschger, P

AU - Klaushofer, K

AU - Altmüller, J

AU - Roy, S

AU - Venkatesh, B

AU - Ganger, R

AU - Grill, F

AU - Ben Chehida, F

AU - Wollnik, B

AU - Altunoglu, U

AU - Al Kaissi, A

AU - Reversade, B

AU - Kaldis, P

A2 - Windpassinger, Christian

PY - 2017

Y1 - 2017

UR - https://www.webofscience.com/wos/woscc/full-record/WOS:000409530900006

UR - https://pubmed.ncbi.nlm.nih.gov/28886341

UR - https://pmc.ncbi.nlm.nih.gov/articles/PMC5591019

U2 - 10.1016/j.ajhg.2017.08.003

DO - 10.1016/j.ajhg.2017.08.003

M3 - Research article

C2 - 28886341

SN - 0002-9297

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

ER -