Point mutations throughout the GL13 gene cause Greig cephalopolysyndactyly syndrome

M Kalff-Suske; A Wild; J Topp; M Wessling; E-M Jacobsen; D Bornholdt; H (Henk) Engel; H Heuer; CM Aalfs; MGEM Ausems; R Barone; A Herzog; P Heutink; T Homfray; G Gillesson-Kaesbach; R König; J Kunze; P Meinecke; D Müller; R Rizzo; S Strenge; A Superti-Furga; K-H Grzeschik

doi:10.1093/hmg/8.9.1769

Point mutations throughout the GL13 gene cause Greig cephalopolysyndactyly syndrome

M Kalff-Suske
, A Wild
, J Topp
, M Wessling
, E-M Jacobsen
, D Bornholdt
, H (Henk) Engel
, H Heuer
, CM Aalfs
, MGEM Ausems
, R Barone
, A Herzog
, P Heutink
, T Homfray
, G Gillesson-Kaesbach
, R König
, J Kunze
, P Meinecke
, D Müller
, R Rizzo

S Strenge, A Superti-Furga, K-H Grzeschik

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

112 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	1769-1777
Number of pages	9
Journal	Human Molecular Genetics
Volume	8
Issue number	9
DOIs	https://doi.org/10.1093/hmg/8.9.1769
Publication status	Published - 1999

Research programs

EMC MGC-02-96-01

Access to Document

10.1093/hmg/8.9.1769

http://hdl.handle.net/1765/55655

Cite this

Kalff-Suske, M., Wild, A., Topp, J., Wessling, M., Jacobsen, E.-M., Bornholdt, D., Engel, H., Heuer, H., Aalfs, CM., Ausems, MGEM., Barone, R., Herzog, A., Heutink, P., Homfray, T., Gillesson-Kaesbach, G., König, R., Kunze, J., Meinecke, P., Müller, D., ... Grzeschik, K.-H. (1999). Point mutations throughout the GL13 gene cause Greig cephalopolysyndactyly syndrome. Human Molecular Genetics, 8(9), 1769-1777. https://doi.org/10.1093/hmg/8.9.1769

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doi = "10.1093/hmg/8.9.1769",

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Kalff-Suske, M, Wild, A, Topp, J, Wessling, M, Jacobsen, E-M, Bornholdt, D, Engel, H, Heuer, H, Aalfs, CM, Ausems, MGEM, Barone, R, Herzog, A, Heutink, P, Homfray, T, Gillesson-Kaesbach, G, König, R, Kunze, J, Meinecke, P, Müller, D, Rizzo, R, Strenge, S, Superti-Furga, A & Grzeschik, K-H 1999, 'Point mutations throughout the GL13 gene cause Greig cephalopolysyndactyly syndrome', Human Molecular Genetics, vol. 8, no. 9, pp. 1769-1777. https://doi.org/10.1093/hmg/8.9.1769

TY - JOUR

T1 - Point mutations throughout the GL13 gene cause Greig cephalopolysyndactyly syndrome

AU - Kalff-Suske, M

AU - Wild, A

AU - Topp, J

AU - Wessling, M

AU - Jacobsen, E-M

AU - Bornholdt, D

AU - Engel, H (Henk)

AU - Heuer, H

AU - Aalfs, CM

AU - Ausems, MGEM

AU - Barone, R

AU - Herzog, A

AU - Heutink, P

AU - Homfray, T

AU - Gillesson-Kaesbach, G

AU - König, R

AU - Kunze, J

AU - Meinecke, P

AU - Müller, D

AU - Rizzo, R

AU - Strenge, S

AU - Superti-Furga, A

AU - Grzeschik, K-H

PY - 1999

Y1 - 1999

U2 - 10.1093/hmg/8.9.1769

DO - 10.1093/hmg/8.9.1769

M3 - Article

SN - 0964-6906

VL - 8

SP - 1769

EP - 1777

JO - Human Molecular Genetics

JF - Human Molecular Genetics

IS - 9

ER -