Browse by UCL people
Group by: Type | Date
Number of items: 6.
Article
Alvizi, L;
Ke, X;
Brito, LA;
Seselgyte, R;
Moore, GE;
Stanier, P;
Passos-Bueno, MR;
(2017)
Differential methylation is associated with non-syndromic cleft lip and palate and contributes to penetrance effects.
Scientific Reports
, 7
, Article 244. 10.1038/s41598-017-02721-0.
|
|
Mangold, E;
Böhmer, AC;
Ishorst, N;
Hoebel, AK;
Gültepe, P;
Schuenke, H;
Klamt, J;
... Ludwig, KU; + view all
(2016)
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate.
American Journal of Human Genetics
, 98
(4)
pp. 755-762.
10.1016/j.ajhg.2016.02.013.
|
|
Seselgyte, R;
Bryant, D;
Demetriou, C;
Ishida, M;
Peskett, E;
Moreno, N;
Morrogh, D;
... Stanier, P; + view all
(2019)
Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family.
Journal of Dental Research
, 98
(6)
pp. 659-665.
10.1177/0022034519837245.
|
|
Sommerlad, B;
Seselgyte, R;
Lees, M;
Pauws, E;
Stanier, P;
Sell, D;
(2019)
Familial absent uvula with velopharyngeal incompetence - a new syndrome?
The Cleft Palate-Craniofacial Journal
10.1177/1055665619880401.
(In press).
|
Book chapter
|
Stanier, PM;
Seselgyte, R;
Moore, GE;
Pauws, E;
(2018)
TBX22-Associated Syndrome.
In:
UNSPECIFIED
(In press).
|
Thesis
|
Seselgyte, Rimante;
(2019)
Clinical and molecular investigation of rare congenital defects of the palate.
Doctoral thesis (Ph.D), UCL (University College London).
|
