Showing results (11-20 of 59) with videos related to

Sort By:
Pageof 6
Acta Paediatrica Scandinavica|July 1, 1989
Lethal respiratory failure in preterm infants due to cystic fibrosis. The first case reportsP M Sharples, P B Colditz, A R Wilkinson
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.
Developmental Medicine and Child Neurology|August 18, 2001
Time costs of caring for children with severe disabilities compared with caring for children without disabilitiesA L Curran, P M Sharples, C White, 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.
BMJ (Clinical Research Ed.)|January 13, 1990
Avoidable factors contributing to death of children with head injuryP M Sharples, A Storey, A Aynsley-Green, 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.
BMJ (Clinical Research Ed.)|November 24, 1990
Causes of fatal childhood accidents involving head injury in northern region, 1979-86P M Sharples, A Storey, A Aynsley-Green, et al.
Pageof 6