A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN

K. Lehmann; P. Seemann; F. Silan; T.O. Goecke; S. Irgang; K.W. Kjær; S. Kjærgaard; M.J. Mahoney; S. Morlot; C. Reissner; B. Kerr; A.O.M. Wilkie; S. Mundlos

A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN

K. Lehmann, P. Seemann, F. Silan, T.O. Goecke, S. Irgang, K.W. Kjær, S. Kjærgaard, M.J. Mahoney, S. Morlot, C. Reissner, B. Kerr, A.O.M. Wilkie, S. Mundlos

Department of Cellular and Molecular Medicine

85 Citations (Scopus)

Abstract

Udgivelsesdato: 2007/8

Original language	English
Journal	American Journal of Human Genetics
Volume	81
Issue number	2
Pages (from-to)	388-396
Number of pages	8
ISSN	0002-9297
Publication status	Published - 2007

Cite this

@article{3865819020ec11ddbc23000ea68e967b,

title = "A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN",

abstract = "Udgivelsesdato: 2007/8",

author = "K. Lehmann and P. Seemann and F. Silan and T.O. Goecke and S. Irgang and K.W. Kj{\ae}r and S. Kj{\ae}rgaard and M.J. Mahoney and S. Morlot and C. Reissner and B. Kerr and A.O.M. Wilkie and S. Mundlos",

year = "2007",

language = "English",

volume = "81",

pages = "388--396",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

number = "2",

}

TY - JOUR

T1 - A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN

AU - Lehmann, K.

AU - Seemann, P.

AU - Silan, F.

AU - Goecke, T.O.

AU - Irgang, S.

AU - Kjær, K.W.

AU - Kjærgaard, S.

AU - Mahoney, M.J.

AU - Morlot, S.

AU - Reissner, C.

AU - Kerr, B.

AU - Wilkie, A.O.M.

AU - Mundlos, S.

PY - 2007

Y1 - 2007

N2 - Udgivelsesdato: 2007/8

AB - Udgivelsesdato: 2007/8

M3 - Journal article

SN - 0002-9297

VL - 81

SP - 388

EP - 396

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 2

ER -