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D R Mowat

Showing results (1-10 of 5) with videos related to

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Journal of Medical Genetics|May 15, 2003
Mowat-Wilson syndromeD R Mowat, M J Wilson, M Goossens
The Medical Journal of Australia|July 23, 1999
Maternal phenylketonuria: a continuing problemD R Mowat, M C Hayden, S M Thompson, et al.
Journal of Paediatrics and Child Health|April 12, 2000
Epilepsy and associated psychopathology in young people with intellectual disabilityJ N Lewis, B J Tonge, D R Mowat, et al.
American Journal of Medical Genetics. Part A|January 7, 2004
Kousseff syndrome: a causally heterogeneous disorderK Maclean, M J Field, A S Colley, et al.
Journal of Medical Genetics|August 27, 1998
Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23D R Mowat, G D Croaker, D T Cass, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Journal of Medical Genetics|May 15, 2003
Mowat-Wilson syndromeD R Mowat, M J Wilson, M Goossens
The Medical Journal of Australia|July 23, 1999
Maternal phenylketonuria: a continuing problemD R Mowat, M C Hayden, S M Thompson, et al.
Journal of Paediatrics and Child Health|April 12, 2000
Epilepsy and associated psychopathology in young people with intellectual disabilityJ N Lewis, B J Tonge, D R Mowat, et al.
American Journal of Medical Genetics. Part A|January 7, 2004
Kousseff syndrome: a causally heterogeneous disorderK Maclean, M J Field, A S Colley, et al.
Journal of Medical Genetics|August 27, 1998
Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23D R Mowat, G D Croaker, D T Cass, et al.
Pageof 1