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Journal of Medical Genetics
|
January 1, 1994
Liver histology in the arthrogryposis multiplex congenita, renal dysfunction, and cholestasis (ARC) syndrome: report of three new cases and review
S P Horslen, O W Quarrell, M S Tanner
American Journal of Medical Genetics
|
February 5, 1998
Baller Gerold syndrome and Fanconi anaemia
O W Quarrell, E L Maltby, C J Harrison
American Journal of Medical Genetics
|
December 1, 1988
Pallister-Killian mosaic syndrome with emphasis on the adult phenotype
O W Quarrell, M A Hamill, H E Hughes
Journal of Medical Genetics
|
March 1, 1988
Absence of close linkage between benign hereditary chorea and the locus D4S10 (probe G8)
O W Quarrell, S Youngman, M Sarfarazi, et al.
Clinical Genetics
|
November 1, 1986
The problem of isolated cases of Huntington's disease in South Wales 1974-1984
O W Quarrell, A Tyler, G Cole, et al.
American Journal of Medical Genetics
|
December 1, 1987
An integrated microcomputer system to maintain a genetic register for Huntington disease
M Sarfarazi, O W Quarrell, G Wolak, et al.
Journal of Medical Genetics
|
January 1, 1990
Interstitial deletion of chromosome 4, del(4)(q12q21.1), in a child with multiple congenital abnormalities
M A Curtis, O W Quarrell, A M Cobon, et al.
Journal of Medical Genetics
|
October 5, 2001
An epidemiological study of Wolf-Hirschhorn syndrome: life expectancy and cause of mortality
N L Shannon, E L Maltby, A S Rigby, et al.
American Journal of Medical Genetics
|
March 2, 1999
Schinzel-Giedion syndrome: evidence for a neurodegenerative process
A M Shah, M F Smith, P D Griffiths, et al.
Clinical Dysmorphology
|
October 1, 1996
A distinct syndrome of familial cleft lip and palate with prominent eyes and characteristic facies in two unrelated families
D Kumar, S Garcia-Minaur, O W Quarrell, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 35) with videos related to
Sort By:
Page
of 4
Journal of Medical Genetics
|
January 1, 1994
Liver histology in the arthrogryposis multiplex congenita, renal dysfunction, and cholestasis (ARC) syndrome: report of three new cases and review
S P Horslen, O W Quarrell, M S Tanner
American Journal of Medical Genetics
|
February 5, 1998
Baller Gerold syndrome and Fanconi anaemia
O W Quarrell, E L Maltby, C J Harrison
American Journal of Medical Genetics
|
December 1, 1988
Pallister-Killian mosaic syndrome with emphasis on the adult phenotype
O W Quarrell, M A Hamill, H E Hughes
Journal of Medical Genetics
|
March 1, 1988
Absence of close linkage between benign hereditary chorea and the locus D4S10 (probe G8)
O W Quarrell, S Youngman, M Sarfarazi, et al.
Clinical Genetics
|
November 1, 1986
The problem of isolated cases of Huntington's disease in South Wales 1974-1984
O W Quarrell, A Tyler, G Cole, et al.
American Journal of Medical Genetics
|
December 1, 1987
An integrated microcomputer system to maintain a genetic register for Huntington disease
M Sarfarazi, O W Quarrell, G Wolak, et al.
Journal of Medical Genetics
|
January 1, 1990
Interstitial deletion of chromosome 4, del(4)(q12q21.1), in a child with multiple congenital abnormalities
M A Curtis, O W Quarrell, A M Cobon, et al.
Journal of Medical Genetics
|
October 5, 2001
An epidemiological study of Wolf-Hirschhorn syndrome: life expectancy and cause of mortality
N L Shannon, E L Maltby, A S Rigby, et al.
American Journal of Medical Genetics
|
March 2, 1999
Schinzel-Giedion syndrome: evidence for a neurodegenerative process
A M Shah, M F Smith, P D Griffiths, et al.
Clinical Dysmorphology
|
October 1, 1996
A distinct syndrome of familial cleft lip and palate with prominent eyes and characteristic facies in two unrelated families
D Kumar, S Garcia-Minaur, O W Quarrell, et al.
Page
of 4