2002/11/205 |
CORGI |
01/09/2020 |
2000/8/122 |
EMBRACE |
31/01/2022 |
1902770 |
Framing of decision-making in predictive and prenatal genetic tests |
31/01/2021 |
1901754 |
Uterine Protection in Lynch Syndrome (UP study) |
31/03/2019 |
1812737 |
BUILD: BAF complex & related genes underlying intellectual disability |
01/10/2020 |
1810701 |
Deep and Frequent Phenotyping |
29/11/2019 |
1804576 |
CORGI 2 |
01/04/2027 |
1801555 |
Spliceosomal Disorders |
31/12/2018 |
1801554 |
BOLT |
10/10/2019 |
1707460 |
EDEN – Early DEvelopment in Neurofibromatosis type 1 |
31/12/2019 |
1707459 |
The SCOTTY Study |
31/05/2021 |
1701371 |
Understanding the conditions of the RAS-MAPK pathway: version 1 |
31/12/2019 |
1701369 |
Genetic disorders of growth, development and the brain |
31/03/2023 |
1701368 |
Genetics of Perrault Syndrome |
30/09/2019 |
1701360 |
Lymres |
31/01/2019 |
1701357 |
POD Study. |
28/02/2019 |
1612341 |
Genes and the Kidney in Tuberous Sclerosis |
31/08/2019 |
1609304 |
Genetic mechanisms in polyposis of the bowel |
31/08/2019 |
1607277 |
ARCI |
21/09/2020 |
1607276 |
Study of rare cutaneous lichenoid, alopecic and scarring variants |
01/09/2025 |
1607274 |
A study of movement disorders in adults with 22q11 deletion syndrome |
01/01/2020 |
1606259 |
Splicing and Disease |
30/11/2022 |
1508124 |
Genetic basis of craniofacial malformations |
31/01/2019 |
1507111 |
IMAGINE. |
30/10/2019 |
1506109 |
A randomised double blind dose non-inferiority trial of aspirin in Lynch syndrome |
31/08/2021 |
1506104 |
Phenotypes in Intellectual Disability |
30/05/2020 |
1504084 |
GENPROS |
01/02/2019 |
1504073 |
Structural Brain Abnormalities and Learning Disability |
31/03/2020 |
1412028 |
INSIGNIA: Exploring mutational signatures in humans |
31/12/2018 |
1310840 |
Genetics of Obesity |
30/11/2022 |
1306796 |
FACT study |
03/12/2020 |
1210707 |
COG – Clinical and Molecular Analyses of Childhood Overgrowth |
12/12/2020 |
1202603 |
HumGenDis |
31/03/2022 |
1201595 |
IDFOW |
01/09/2020 |