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Journal of Genetic Counseling
|
May 3, 2007
Risky communication: pitfalls in counseling about risk, and how to avoid them
K O'Doherty, G K Suthers
American Journal of Human Genetics
|
July 1, 1990
Genetic counseling in rare syndromes: a resampling method for determining an approximate confidence interval for gene location with linkage data from a single pedigree
G K Suthers, S R Wilson
American Journal of Medical Genetics
|
August 1, 1988
Ring chromosome 11 and café-au-lait spots
K Fagan, G K Suthers, G Hardacre
American Journal of Medical Genetics
|
May 1, 1988
Fragile X syndrome and nephrogenic diabetes insipidus
G K Suthers, G Turner, J C Mulley
American Journal of Medical Genetics
|
May 1, 1988
A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14
G K Suthers, G Turner, J C Mulley
Australian Paediatric Journal
|
August 1, 1987
Control of nephroblastoma: associated hypertension and polydipsia by captopril
G K Suthers, L P Roy, M Stevens
Clinical Dysmorphology
|
October 1, 1993
A distinctive syndrome of brachycephaly, deafness, cataracts and mental retardation
G K Suthers, A E Earley, S M Huson
Journal of Medical Genetics
|
December 24, 2005
Letting the family know: balancing ethics and effectiveness when notifying relatives about genetic testing for a familial disorder
G K Suthers, J Armstrong, J McCormack, et al.
Journal of Medical Genetics
|
August 3, 2005
Arteriovenous malformations in Cowden syndrome
M M Turnbull, V Humeniuk, B Stein, et al.
Journal of Medical Genetics
|
April 1, 1989
Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigree
G K Suthers, J I Manson, L M Stern, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 29) with videos related to
Sort By:
Page
of 3
Journal of Genetic Counseling
|
May 3, 2007
Risky communication: pitfalls in counseling about risk, and how to avoid them
K O'Doherty, G K Suthers
American Journal of Human Genetics
|
July 1, 1990
Genetic counseling in rare syndromes: a resampling method for determining an approximate confidence interval for gene location with linkage data from a single pedigree
G K Suthers, S R Wilson
American Journal of Medical Genetics
|
August 1, 1988
Ring chromosome 11 and café-au-lait spots
K Fagan, G K Suthers, G Hardacre
American Journal of Medical Genetics
|
May 1, 1988
Fragile X syndrome and nephrogenic diabetes insipidus
G K Suthers, G Turner, J C Mulley
American Journal of Medical Genetics
|
May 1, 1988
A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14
G K Suthers, G Turner, J C Mulley
Australian Paediatric Journal
|
August 1, 1987
Control of nephroblastoma: associated hypertension and polydipsia by captopril
G K Suthers, L P Roy, M Stevens
Clinical Dysmorphology
|
October 1, 1993
A distinctive syndrome of brachycephaly, deafness, cataracts and mental retardation
G K Suthers, A E Earley, S M Huson
Journal of Medical Genetics
|
December 24, 2005
Letting the family know: balancing ethics and effectiveness when notifying relatives about genetic testing for a familial disorder
G K Suthers, J Armstrong, J McCormack, et al.
Journal of Medical Genetics
|
August 3, 2005
Arteriovenous malformations in Cowden syndrome
M M Turnbull, V Humeniuk, B Stein, et al.
Journal of Medical Genetics
|
April 1, 1989
Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigree
G K Suthers, J I Manson, L M Stern, et al.
Page
of 3