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Bhaskar, Sanjeev
172  results:
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1

Unforgotten: S5:

Wilson, Andy ; Lancel, Andrew ; Main, Carolina... , 2023
Link: https://unibremen.kanopy..
 
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2

Stath Lets Flats: S3:

Gaynord, Andrew ; Lancel, Andrew ; Main, Carolina... , 2021
Link: https://unibremen.kanopy..
 
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3

Unforgotten: S4:

Wilson, Andy ; Walker, Nicola ; Bhaskar, Sanjeev , 2021
Link: https://unibremen.kanopy..
 
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4

Unforgotten: S3:

Wilson, Andy ; Jennings, Alex ; Fleet, James... , 2018
Link: https://unibremen.kanopy..
 
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5

Unforgotten: S2:

Wilson, Andy ; Timimi, Badria ; Ashbourne, Lorraine... , 2017
Link: https://unibremen.kanopy..
 
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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/..
 
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7

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/..
 
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8

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/..
 
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9

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/..
 
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10

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/..
 
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11

Unforgotten: S1:

Wilson, Andy ; Hill, Bernard ; Jones, Gemma... , 2015
Link: https://unibremen.kanopy..
 
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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/..
 
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13

Unforgotten:

Wilson, Andy ; Hill, Bernard ; Jones, Gemma... , 2015
Link: https://unibremen.kanopy..
 
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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/..
 
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15

Autozygosity Mapping with Exome Sequence Data:

Carr, Ian M. ; Bhaskar, Sanjeev ; O' Sullivan, James...
Human Mutation.  34 (2012)  1 - p. 50-56 , 2012
Link: https://doi.org/10.1002/..
 
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