Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23
Mowat, D R, Croaker, G D, Cass, D T, Kerr, B A, Chaitow, J, Adès, L C, Chia, N L, Wilson, M J
Published in Journal of medical genetics (01.08.1998)
Published in Journal of medical genetics (01.08.1998)
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Kousseff syndrome: A causally heterogeneous disorder
Maclean, K., Field, M.J., Colley, A.S., Mowat, D.R., Sparrow, D.B., Dunwoodie, S.L., Kirk, E.P.E.
Published in American journal of medical genetics. Part A (30.01.2004)
Published in American journal of medical genetics. Part A (30.01.2004)
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Epilepsy and associated psychopathology in young people with intellectual disability
LEWIS, JN, TONGE, BJ, MOWAT, DR, EINFELD, Sl, SIDDONS, HM, REES, VW
Published in Journal of paediatrics and child health (01.04.2000)
Published in Journal of paediatrics and child health (01.04.2000)
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Maternal phenylketonuria: a continuing problem
Mowat, D R, Hayden, M C, Thompson, S M, Wilcken, B
Published in Medical journal of Australia (21.06.1999)
Published in Medical journal of Australia (21.06.1999)
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Journal Article
DERIVADOS DE PIRROLOPIRIDINA SUSTITUIDOS
Dr. Rafael CARRETERO, Dr. Bernd BUCHMANN, Dra. Gabriele LEDER, Dr. Roland NEUHAUS, Dra. Kirstin PETERSEN, Robin Michael MEIER, Dra. Nuria AIGUABELLA FONT, Dra. Sandra BERNDT, Dr. Olaf PANKNIN, Dr. Jeffrey Stuart MOWAT, OFFRINGA Rienk
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Year of Publication 28.02.2019
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