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Journal of Medical Ethics
|
September 2, 2008
Genetic research on rare familial disorders: consent and the blurred boundaries between clinical service and research
M Ponder, H Statham, N Hallowell, et al.
Clinical Dysmorphology
|
April 18, 1998
Four cases of amelia of the upper limb associated with anal atresia--is this VACTERL with extreme limb involvement?
S M Price, A C Berry, F L Raymond, et al.
Journal of Medical Genetics
|
September 10, 2003
Neurofibromatosis 2 in a patient with a de novo balanced reciprocal translocation 46,X,t(X;22)(p11.2;q11.2)
C Bovie, S T Holden, A Schroer, et al.
Journal of Medical Genetics
|
April 16, 1998
A new approach to the elucidation of complex chromosome rearrangements illustrated by a case of Rieger syndrome
C M Ogilvie, F L Raymond, R H Harrison, et al.
Biochemical Society Transactions
|
August 1, 1983
Antigenic variation in influenza virus
A J Caton, F L Raymond, G G Brownlee, et al.
Nucleic Acids Research
|
October 25, 1983
Antigenicity and evolution amongst recent influenza viruses of H1N1 subtype
F L Raymond, A J Caton, N J Cox, et al.
Virology
|
January 30, 1986
The antigenicity and evolution of influenza H1 haemagglutinin, from 1950-1957 and 1977-1983: two pathways from one gene
F L Raymond, A J Caton, N J Cox, et al.
Journal of Intellectual Disability Research : JIDR
|
April 18, 2019
Mental health and behavioural problems in children with XXYY: a comparison with intellectual disabilities
R Srinivasan, J Wolstencroft, M Erwood, et al.
Frontiers in Genetics
|
February 14, 2018
Functional Analyses of a Novel Splice Variant in the <i>CHD7</i> Gene, Found by Next Generation Sequencing, Confirm Its Pathogenicity in a Spanish Patient and Diagnose Him with CHARGE Syndrome
Olatz Villate, Nekane Ibarluzea, Eugenia Fraile-Bethencourt, et al.
Clinical Genetics
|
November 15, 2006
Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardation
M Field, P Tarpey, J Boyle, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 26) with videos related to
Sort By:
Page
of 3
Journal of Medical Ethics
|
September 2, 2008
Genetic research on rare familial disorders: consent and the blurred boundaries between clinical service and research
M Ponder, H Statham, N Hallowell, et al.
Clinical Dysmorphology
|
April 18, 1998
Four cases of amelia of the upper limb associated with anal atresia--is this VACTERL with extreme limb involvement?
S M Price, A C Berry, F L Raymond, et al.
Journal of Medical Genetics
|
September 10, 2003
Neurofibromatosis 2 in a patient with a de novo balanced reciprocal translocation 46,X,t(X;22)(p11.2;q11.2)
C Bovie, S T Holden, A Schroer, et al.
Journal of Medical Genetics
|
April 16, 1998
A new approach to the elucidation of complex chromosome rearrangements illustrated by a case of Rieger syndrome
C M Ogilvie, F L Raymond, R H Harrison, et al.
Biochemical Society Transactions
|
August 1, 1983
Antigenic variation in influenza virus
A J Caton, F L Raymond, G G Brownlee, et al.
Nucleic Acids Research
|
October 25, 1983
Antigenicity and evolution amongst recent influenza viruses of H1N1 subtype
F L Raymond, A J Caton, N J Cox, et al.
Virology
|
January 30, 1986
The antigenicity and evolution of influenza H1 haemagglutinin, from 1950-1957 and 1977-1983: two pathways from one gene
F L Raymond, A J Caton, N J Cox, et al.
Journal of Intellectual Disability Research : JIDR
|
April 18, 2019
Mental health and behavioural problems in children with XXYY: a comparison with intellectual disabilities
R Srinivasan, J Wolstencroft, M Erwood, et al.
Frontiers in Genetics
|
February 14, 2018
Functional Analyses of a Novel Splice Variant in the <i>CHD7</i> Gene, Found by Next Generation Sequencing, Confirm Its Pathogenicity in a Spanish Patient and Diagnose Him with CHARGE Syndrome
Olatz Villate, Nekane Ibarluzea, Eugenia Fraile-Bethencourt, et al.
Clinical Genetics
|
November 15, 2006
Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardation
M Field, P Tarpey, J Boyle, et al.
Page
of 3