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British Medical Journal
|
October 9, 1971
Chromosome analysis before birth and its value in genetic counselling
M E Ferguson-Smith, M A Ferguson-Smith, N C Nevin, et al.
Biology and Society : the Journal of the Eugenics Society
|
June 1, 1987
Report of the delegation of clinical geneticists to China, Spring 1986
M Laurence, P S Harper, R Harris, et al.
The Journal of Investigative Dermatology
|
December 24, 1997
A novel mutation in the helix termination peptide of keratin 5 causing epidermolysis bullosa simplex Dowling-Meara
A D Irvine, K E McKenna, A Bingham, et al.
The British Journal of Dermatology
|
October 1, 1972
Atypical erythrokeratoderma with deafness, physical retardation and peripheral neuropathy
J M Beare, N C Nevin, P Froggatt, et al.
Lancet (London, England)
|
May 12, 1990
Prenatal diagnosis of mucolipidosis II by early amniocentesis
G T Besley, D M Broadhead, N C Nevin, et al.
The British Journal of Ophthalmology
|
August 1, 1992
Prenatal exclusion of Norrie's disease
R M Redmond, C A Graham, E D Kelly, et al.
American Journal of Medical Genetics
|
April 11, 2000
First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH
M Bhat, P J Morrison, A Getty, et al.
Human Mutation
|
January 1, 1994
Non-phenylketonuria hyperphenylalaninaemia in Northern Ireland: frequent mutation allows screening and early diagnosis
J Zschocke, C A Graham, F J Stewart, et al.
Biochemical Society Transactions
|
April 1, 1990
Localization of a human fibroblast extracellular protein in cells and tissues by monoclonal antibody
W H McLean, J C Orchin, H Foster, et al.
The British Journal of Dermatology
|
February 1, 1982
Letterer-Siwe disease: a study of thirteen cases over a 21 - year period
E A Bingham, J M Bridges, A M Kelly, et al.
Page
of 23
Search research articles
Search
Showing results (151-160 of 223) with videos related to
Sort By:
Page
of 23
British Medical Journal
|
October 9, 1971
Chromosome analysis before birth and its value in genetic counselling
M E Ferguson-Smith, M A Ferguson-Smith, N C Nevin, et al.
Biology and Society : the Journal of the Eugenics Society
|
June 1, 1987
Report of the delegation of clinical geneticists to China, Spring 1986
M Laurence, P S Harper, R Harris, et al.
The Journal of Investigative Dermatology
|
December 24, 1997
A novel mutation in the helix termination peptide of keratin 5 causing epidermolysis bullosa simplex Dowling-Meara
A D Irvine, K E McKenna, A Bingham, et al.
The British Journal of Dermatology
|
October 1, 1972
Atypical erythrokeratoderma with deafness, physical retardation and peripheral neuropathy
J M Beare, N C Nevin, P Froggatt, et al.
Lancet (London, England)
|
May 12, 1990
Prenatal diagnosis of mucolipidosis II by early amniocentesis
G T Besley, D M Broadhead, N C Nevin, et al.
The British Journal of Ophthalmology
|
August 1, 1992
Prenatal exclusion of Norrie's disease
R M Redmond, C A Graham, E D Kelly, et al.
American Journal of Medical Genetics
|
April 11, 2000
First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH
M Bhat, P J Morrison, A Getty, et al.
Human Mutation
|
January 1, 1994
Non-phenylketonuria hyperphenylalaninaemia in Northern Ireland: frequent mutation allows screening and early diagnosis
J Zschocke, C A Graham, F J Stewart, et al.
Biochemical Society Transactions
|
April 1, 1990
Localization of a human fibroblast extracellular protein in cells and tissues by monoclonal antibody
W H McLean, J C Orchin, H Foster, et al.
The British Journal of Dermatology
|
February 1, 1982
Letterer-Siwe disease: a study of thirteen cases over a 21 - year period
E A Bingham, J M Bridges, A M Kelly, et al.
Page
of 23