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Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate.
33 auth.
E. Mangold,
A. Böhmer,
N. Ishorst,
Ann-Kathrin Hoebel,
Pinar Gültepe,
Hannah Schuenke,
J. Klamt,
A. Hofmann,
L. Gölz,
R. Raff,
P. Tessmann,
S. Nowak,
H. Reutter,
A. Hemprich,
T. Kreusch,
...
F. Kramer,
B. Braumann,
R. Reich,
G. Schmidt,
A. Jäger,
R. Reiter,
S. Brosch,
J. Stavusis,
M. Ishida,
R. Seselgyte,
G. Moore,
M. Nöthen,
G. Borck,
Khalid Aldhorae,
B. Lāce,
P. Stanier,
M. Knapp,
K. Ludwig
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6 |
2016 |
6 🐜
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Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing
31 auth.
Ann-Kathrin Hoebel,
D. Drichel,
D. Drichel,
M. Vorst,
Anne C. Böhmer,
S. Sivalingam,
N. Ishorst,
J. Klamt,
Lina Gölz,
M. Alblas,
A. Maaser,
Kathleen Keppler,
A. Zink,
M. J. Dixon,
Jill Dixon,
...
Alexander Hemprich,
Teresa Kruse,
I. Graf,
A. Dunsche,
G. Schmidt,
N. Daratsianos,
S. Nowak,
Khalid Aldhorae,
M. Nöthen,
Michael Knapp,
Holger Thiele,
C. Gilissen,
H. Reutter,
A. Hoischen,
E. Mangold,
K. Ludwig
|
5 |
2017 |
5 🦁
|
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Further evidence for deletions in 7p14.1 contributing to nonsyndromic cleft lip with or without cleft palate.
16 auth.
J. Klamt,
A. Hofmann,
A. Böhmer,
Ann-Kathrin Hoebel,
L. Gölz,
J. Becker,
A. Zink,
Markus Draaken,
A. Hemprich,
M. Scheer,
...
G. Schmidt,
M. Martini,
M. Knapp,
E. Mangold,
F. Degenhardt,
K. Ludwig
|
2 |
2016 |
2 🐜
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