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Bhaskar, Sanjeev
172
results:
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Online (172)
Mediatypes
Articles (Online) (74)
Bookchapter (Online) (10)
OpenAccess-fulltext (81)
Video (Online) (7)
Sorted by: Relevance
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?
1
Unforgotten: S5:
Wilson, Andy
;
Lancel, Andrew
;
Main, Carolina
... , 2023
Link:
https://unibremen.kanopy..
?
2
Stath Lets Flats: S3:
Gaynord, Andrew
;
Lancel, Andrew
;
Main, Carolina
... , 2021
Link:
https://unibremen.kanopy..
?
3
Unforgotten: S4:
Wilson, Andy
;
Walker, Nicola
;
Bhaskar, Sanjeev
, 2021
Link:
https://unibremen.kanopy..
?
4
Unforgotten: S3:
Wilson, Andy
;
Jennings, Alex
;
Fleet, James
... , 2018
Link:
https://unibremen.kanopy..
?
5
Validation of copy number variation analysis for next-gener..:
Ellingford, Jamie M
;
Campbell, Christopher
;
Barton, Stephanie
...
European Journal of Human Genetics. 25 (2017) 6 - p. 719-724 , 2017
Link:
https://doi.org/10.1038/..
?
6
ACTB Loss-of-Function Mutations Result in a Pleiotropic Dev..:
Cuvertino, Sara
;
Stuart, Helen M.
;
Chandler, Kate E.
...
The American Journal of Human Genetics. 101 (2017) 6 - p. 1021-1033 , 2017
Link:
https://doi.org/10.1016/..
?
7
Unforgotten: S2:
Wilson, Andy
;
Timimi, Badria
;
Ashbourne, Lorraine
... , 2017
Link:
https://unibremen.kanopy..
?
8
Whole Genome Sequencing Increases Molecular Diagnostic Yiel..:
Ellingford, Jamie M.
;
Barton, Stephanie
;
Bhaskar, Sanjeev
...
Ophthalmology. 123 (2016) 5 - p. 1143-1150 , 2016
Link:
https://doi.org/10.1016/..
?
9
Non lethal Raine syndrome and differential diagnosis:
Elalaoui, Siham Chafai
;
Al-Sheqaih, Nada
;
Ratbi, Ilham
...
European Journal of Medical Genetics. 59 (2016) 11 - p. 577-583 , 2016
Link:
https://doi.org/10.1016/..
?
10
Exploring the genetic basis of 3MC syndrome: Findings in 12..:
Urquhart, Jill
;
Roberts, Rebecca
;
de Silva, Deepthi
...
American Journal of Medical Genetics Part A. 170 (2016) 5 - p. 1216-1224 , 2016
Link:
https://doi.org/10.1002/..
?
11
Unforgotten: S1:
Wilson, Andy
;
Hill, Bernard
;
Jones, Gemma
... , 2015
Link:
https://unibremen.kanopy..
?
12
A reliable method for the detection of BRCA1 and BRCA2 muta..:
Ellison, Gillian
;
Huang, Shuwen
;
Carr, Hedley
...
BMC Clinical Pathology. 15 (2015) 1 - p. , 2015
Link:
https://doi.org/10.1186/..
?
13
Unforgotten:
Wilson, Andy
;
Hill, Bernard
;
Jones, Gemma
... , 2015
Link:
https://unibremen.kanopy..
?
14
LRIG2 Mutations Cause Urofacial Syndrome:
Stuart, Helen M.
;
Roberts, Neil A.
;
Burgu, Berk
...
The American Journal of Human Genetics. 92 (2013) 2 - p. 259-264 , 2013
Link:
https://doi.org/10.1016/..
?
15
Early Diagnosis of Werner's Syndrome Using Exome-Wide Seque..:
Semple, Robert K.
;
Barroso, Inês
;
O'Rahilly, Stephen
...
Frontiers in Endocrinology. 2 (2011) - p. , 2011
Link:
https://doi.org/10.3389/..
1-15