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Cytogenetics and Cell Genetics
|
January 1, 1978
Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7
E J Winsor, C G Palmer, P M Ellis, et al.
Clinical Genetics
|
November 1, 1986
Full expression of Hunter's disease in a female with an X-chromosome deletion leading to non-random inactivation
D M Broadhead, J M Kirk, A J Burt, et al.
Clinical Genetics
|
July 1, 1989
An aetiological study of isochromosome-X Turner's syndrome
A D Carothers, R De Mey, M Daker, et al.
Breast (Edinburgh, Scotland)
|
January 21, 2004
Doctors' participation in randomized trials of adjuvant systemic therapy in breast cancer: how does it relate to their recommendations for standard therapy in breast cancer?
P M Ellis, P N Buttow, R J Simes, et al.
Prenatal Diagnosis
|
June 1, 1994
Prenatal diagnosis of fragile X syndrome: management of the male fetus with a premutation
L Strain, M E Porteous, C M Gosden, et al.
Birth Defects Original Article Series
|
January 1, 1975
Centromeric linkage
M A Ferguson-Smith, P M Ellis, O Mutchinick, et al.
Genetic Epidemiology
|
February 25, 1999
Trends in prenatal diagnosis of Down syndrome and other autosomal trisomies in Scotland 1990 to 1994, with associated cytogenetic and epidemiological findings
A D Carothers, E Boyd, G Lowther, et al.
Cytogenetics and Cell Genetics
|
January 1, 1975
Centromeric linkage
M A Ferguson-Smith, P M Ellis, O Mutchinick, et al.
Clinical Oncology (Royal College of Radiologists (Great Britain))
|
July 16, 2018
Guideline for the Initial Management of Small Cell Lung Cancer (Limited and Extensive Stage) and the Role of Thoracic Radiotherapy and First-line Chemotherapy
A Sun, L D Durocher-Allen, P M Ellis, et al.
Current Oncology (Toronto, Ont.)
|
September 25, 2019
Resource use in the last three months of life by lung cancer patients in southern Ontario
Y Wang, A Van Dam, M Slaven, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 93) with videos related to
Sort By:
Page
of 10
Cytogenetics and Cell Genetics
|
January 1, 1978
Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7
E J Winsor, C G Palmer, P M Ellis, et al.
Clinical Genetics
|
November 1, 1986
Full expression of Hunter's disease in a female with an X-chromosome deletion leading to non-random inactivation
D M Broadhead, J M Kirk, A J Burt, et al.
Clinical Genetics
|
July 1, 1989
An aetiological study of isochromosome-X Turner's syndrome
A D Carothers, R De Mey, M Daker, et al.
Breast (Edinburgh, Scotland)
|
January 21, 2004
Doctors' participation in randomized trials of adjuvant systemic therapy in breast cancer: how does it relate to their recommendations for standard therapy in breast cancer?
P M Ellis, P N Buttow, R J Simes, et al.
Prenatal Diagnosis
|
June 1, 1994
Prenatal diagnosis of fragile X syndrome: management of the male fetus with a premutation
L Strain, M E Porteous, C M Gosden, et al.
Birth Defects Original Article Series
|
January 1, 1975
Centromeric linkage
M A Ferguson-Smith, P M Ellis, O Mutchinick, et al.
Genetic Epidemiology
|
February 25, 1999
Trends in prenatal diagnosis of Down syndrome and other autosomal trisomies in Scotland 1990 to 1994, with associated cytogenetic and epidemiological findings
A D Carothers, E Boyd, G Lowther, et al.
Cytogenetics and Cell Genetics
|
January 1, 1975
Centromeric linkage
M A Ferguson-Smith, P M Ellis, O Mutchinick, et al.
Clinical Oncology (Royal College of Radiologists (Great Britain))
|
July 16, 2018
Guideline for the Initial Management of Small Cell Lung Cancer (Limited and Extensive Stage) and the Role of Thoracic Radiotherapy and First-line Chemotherapy
A Sun, L D Durocher-Allen, P M Ellis, et al.
Current Oncology (Toronto, Ont.)
|
September 25, 2019
Resource use in the last three months of life by lung cancer patients in southern Ontario
Y Wang, A Van Dam, M Slaven, et al.
Page
of 10