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P W Lunt

Showing results (11-20 of 44) with videos related to

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Journal of Medical Genetics|February 24, 2001
Distal trisomy 2p and arachnodactylyD J Stalker, S Vigneswaren, P M Sharples, et al.
Journal of Medical Genetics|January 1, 1993
Holoprosencephaly: a family showing dominant inheritance and variable expressionA L Collins, P W Lunt, C Garrett, et al.
Journal of Medical Genetics|August 1, 1989
A genetic linkage study of facioscapulohumeral (Landouzy-Déjérine) disease with 24 polymorphic DNA probesM Upadhyaya, M Sarfarazi, P W Lunt, et al.
Neuromuscular Disorders : NMD|September 1, 1994
A scapular onset muscular dystrophy without facial involvement: possible allelism with facioscapulohumeral muscular dystrophyP E Jardine, M Upadhyaya, J Maynard, et al.
Journal of the Neurological Sciences|December 1, 1988
Evidence against location of the gene for facioscapulohumeral muscular dystrophy on the distal long arm of chromosome 14P W Lunt, J G Noades, M Upadhyaya, et al.
Clinical Dysmorphology|July 1, 1993
Partial 6q monosomy/partial 12q trisomy in a child with features of Kabuki make-up syndromeP E Jardine, L C Burvill-Holmes, W H Schutt, et al.
Journal of Medical Genetics|August 28, 1999
A new family linked to the RP1 dominant retinitis pigmentosa locus on chromosome 8qC F Inglehearn, J C McHale, T J Keen, et al.
Journal of the Royal Society of Medicine|August 1, 1993
A case illustrating Proteus and Klippel-Trenaunay syndrome overlapJ E Sansom, P Jardine, P W Lunt, et al.
Clinical Dysmorphology|April 1, 1993
Oculo-auriculo-vertebral spectrum with vascular ring and other unusual anomaliesM P Richardson, P W Lunt, N Marlow, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 4, 2000
Prenatal onset spinal muscular atrophyM J MacLeod, J E Taylor, P W Lunt, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
Journal of Medical Genetics|February 24, 2001
Distal trisomy 2p and arachnodactylyD J Stalker, S Vigneswaren, P M Sharples, et al.
Journal of Medical Genetics|January 1, 1993
Holoprosencephaly: a family showing dominant inheritance and variable expressionA L Collins, P W Lunt, C Garrett, et al.
Journal of Medical Genetics|August 1, 1989
A genetic linkage study of facioscapulohumeral (Landouzy-Déjérine) disease with 24 polymorphic DNA probesM Upadhyaya, M Sarfarazi, P W Lunt, et al.
Neuromuscular Disorders : NMD|September 1, 1994
A scapular onset muscular dystrophy without facial involvement: possible allelism with facioscapulohumeral muscular dystrophyP E Jardine, M Upadhyaya, J Maynard, et al.
Journal of the Neurological Sciences|December 1, 1988
Evidence against location of the gene for facioscapulohumeral muscular dystrophy on the distal long arm of chromosome 14P W Lunt, J G Noades, M Upadhyaya, et al.
Clinical Dysmorphology|July 1, 1993
Partial 6q monosomy/partial 12q trisomy in a child with features of Kabuki make-up syndromeP E Jardine, L C Burvill-Holmes, W H Schutt, et al.
Journal of Medical Genetics|August 28, 1999
A new family linked to the RP1 dominant retinitis pigmentosa locus on chromosome 8qC F Inglehearn, J C McHale, T J Keen, et al.
Journal of the Royal Society of Medicine|August 1, 1993
A case illustrating Proteus and Klippel-Trenaunay syndrome overlapJ E Sansom, P Jardine, P W Lunt, et al.
Clinical Dysmorphology|April 1, 1993
Oculo-auriculo-vertebral spectrum with vascular ring and other unusual anomaliesM P Richardson, P W Lunt, N Marlow, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 4, 2000
Prenatal onset spinal muscular atrophyM J MacLeod, J E Taylor, P W Lunt, et al.
Pageof 5