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D T Cass

Showing results (61-70 of 65) with videos related to

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The Medical Journal of Australia|May 16, 1994
Postnatal diagnosis and outcome of urinary tract abnormalities detected by antenatal ultrasoundJ C Tam, E M Hodson, K K Choong, 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.
Nature Genetics|August 1, 1993
A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10M Angrist, E Kauffman, S A Slaugenhaupt, et al.
Annals of Human Genetics|December 18, 2007
Evaluation of the NK2 homeobox 1 gene (NKX2-1) as a Hirschsprung's disease locusM-M Garcia-Barceló, D K Lau, E S Ngan, et al.
Human Mutation|January 1, 1997
Frequency of RET mutations in long- and short-segment Hirschsprung diseaseM Seri, L Yin, V Barone, et al.
Pageof 7

Showing results (61-70 of 65) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 65 results.
The Medical Journal of Australia|May 16, 1994
Postnatal diagnosis and outcome of urinary tract abnormalities detected by antenatal ultrasoundJ C Tam, E M Hodson, K K Choong, 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.
Nature Genetics|August 1, 1993
A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10M Angrist, E Kauffman, S A Slaugenhaupt, et al.
Annals of Human Genetics|December 18, 2007
Evaluation of the NK2 homeobox 1 gene (NKX2-1) as a Hirschsprung's disease locusM-M Garcia-Barceló, D K Lau, E S Ngan, et al.
Human Mutation|January 1, 1997
Frequency of RET mutations in long- and short-segment Hirschsprung diseaseM Seri, L Yin, V Barone, et al.
Pageof 7