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Journal of Medical Genetics
|
March 1, 1992
Prenatal diagnosis and presymptomatic detection of neurofibromatosis type 1
M Upadhyaya, A Fryer, J MacMillan, et al.
Clinical Dysmorphology
|
July 1, 1996
Three infants of diabetic mothers with malformations of left-right asymmetry--further evidence for the aetiological role of diabetes in this malformation spectrum
A Slavotinek, E Hellen, S Gould, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 1, 1997
Spinal and cutaneous schwannomatosis is a variant form of type 2 neurofibromatosis: a clinical and molecular study
D G Evans, S Mason, S M Huson, et al.
Journal of the Neurological Sciences
|
May 8, 2000
Diagnostic re-evaluation of a case of 'cerebellar atrophy with Huntington's disease'
S M White, S S Gubbay, C G Norbury, et al.
The Journal of Laryngology and Otology
|
May 1, 1993
Type 2 neurofibromatosis: the need for supraregional care?
D G Evans, R Ramsden, S M Huson, et al.
Human Genetics
|
July 1, 1989
MASA syndrome: further clinical delineation and chromosomal localisation
R M Winter, K E Davies, M V Bell, et al.
Human Molecular Genetics
|
December 1, 1992
Analysis of mutations at the neurofibromatosis 1 (NF1) locus
M Upadhyaya, M Shen, A Cherryson, et al.
The Quarterly Journal of Medicine
|
August 1, 1992
A clinical study of type 2 neurofibromatosis
D G Evans, S M Huson, D Donnai, et al.
Clinical Genetics
|
May 2, 2007
Should NF2 mutation screening be undertaken in patients with an apparently isolated vestibular schwannoma?
D G R Evans, R T Ramsden, C Gokhale, et al.
Lancet (London, England)
|
July 1, 1995
Arthrogryposis multiplex congenita with maternal autoantibodies specific for a fetal antigen
A Vincent, C Newland, L Brueton, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 85) with videos related to
Sort By:
Page
of 9
Journal of Medical Genetics
|
March 1, 1992
Prenatal diagnosis and presymptomatic detection of neurofibromatosis type 1
M Upadhyaya, A Fryer, J MacMillan, et al.
Clinical Dysmorphology
|
July 1, 1996
Three infants of diabetic mothers with malformations of left-right asymmetry--further evidence for the aetiological role of diabetes in this malformation spectrum
A Slavotinek, E Hellen, S Gould, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 1, 1997
Spinal and cutaneous schwannomatosis is a variant form of type 2 neurofibromatosis: a clinical and molecular study
D G Evans, S Mason, S M Huson, et al.
Journal of the Neurological Sciences
|
May 8, 2000
Diagnostic re-evaluation of a case of 'cerebellar atrophy with Huntington's disease'
S M White, S S Gubbay, C G Norbury, et al.
The Journal of Laryngology and Otology
|
May 1, 1993
Type 2 neurofibromatosis: the need for supraregional care?
D G Evans, R Ramsden, S M Huson, et al.
Human Genetics
|
July 1, 1989
MASA syndrome: further clinical delineation and chromosomal localisation
R M Winter, K E Davies, M V Bell, et al.
Human Molecular Genetics
|
December 1, 1992
Analysis of mutations at the neurofibromatosis 1 (NF1) locus
M Upadhyaya, M Shen, A Cherryson, et al.
The Quarterly Journal of Medicine
|
August 1, 1992
A clinical study of type 2 neurofibromatosis
D G Evans, S M Huson, D Donnai, et al.
Clinical Genetics
|
May 2, 2007
Should NF2 mutation screening be undertaken in patients with an apparently isolated vestibular schwannoma?
D G R Evans, R T Ramsden, C Gokhale, et al.
Lancet (London, England)
|
July 1, 1995
Arthrogryposis multiplex congenita with maternal autoantibodies specific for a fetal antigen
A Vincent, C Newland, L Brueton, et al.
Page
of 9