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Human Genetics
|
June 9, 1978
Interstitial deletion of chromosome 7 detected in three unrelated patients
M Seabright, G M Lewis
Human Genetics
|
September 22, 1977
Two cases of trisomy 21 and one XXY case with atypical clinical features
A Hobbs, M Seabright, S Mould
Humangenetik
|
August 29, 1975
Variation in trypsin banding at different stages of contraction in human chromosomes and the definition, by measurement, of the "average" karyotype
M Seabright, P Cooke, M Wheeler
Human Genetics
|
December 15, 1976
Trisomy 9 associated with an enlarged 9qh segment in a liveborn
M Seabright, N Gregson, S Mould
Humangenetik
|
July 23, 1975
The differential distribution of X-ray induced chromosome lesions in trypsin-banded preparations from human subjects
P Cooke, M Seabright, M Wheeler
Journal of Medical Genetics
|
December 1, 1980
A familial polymorphic variant of chromosome 5
M Seabright, N M Gregson, M Johnson
Journal of Medical Genetics
|
August 1, 1980
Pericentric inversion (13) with two different recombinants in the same family
E M Williamson, J F Miller, M Seabright
Archives of Disease in Childhood
|
March 1, 1986
Chromosome abnormalities in pupils attending ESN/M schools
M A Lamont, N R Dennis, M Seabright
Human Genetics
|
April 24, 1978
A further case of a 22;22 Robertsonian translocation associated with recurrent abortions
M Mameli, S Cardia, A Milia, et al.
Journal of Medical Genetics
|
February 1, 1985
The prevalence of translocations in parents of children with regular trisomy 21: a possible interchromosomal effect?
R H Lindenbaum, M Hultén, A McDermott, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Human Genetics
|
June 9, 1978
Interstitial deletion of chromosome 7 detected in three unrelated patients
M Seabright, G M Lewis
Human Genetics
|
September 22, 1977
Two cases of trisomy 21 and one XXY case with atypical clinical features
A Hobbs, M Seabright, S Mould
Humangenetik
|
August 29, 1975
Variation in trypsin banding at different stages of contraction in human chromosomes and the definition, by measurement, of the "average" karyotype
M Seabright, P Cooke, M Wheeler
Human Genetics
|
December 15, 1976
Trisomy 9 associated with an enlarged 9qh segment in a liveborn
M Seabright, N Gregson, S Mould
Humangenetik
|
July 23, 1975
The differential distribution of X-ray induced chromosome lesions in trypsin-banded preparations from human subjects
P Cooke, M Seabright, M Wheeler
Journal of Medical Genetics
|
December 1, 1980
A familial polymorphic variant of chromosome 5
M Seabright, N M Gregson, M Johnson
Journal of Medical Genetics
|
August 1, 1980
Pericentric inversion (13) with two different recombinants in the same family
E M Williamson, J F Miller, M Seabright
Archives of Disease in Childhood
|
March 1, 1986
Chromosome abnormalities in pupils attending ESN/M schools
M A Lamont, N R Dennis, M Seabright
Human Genetics
|
April 24, 1978
A further case of a 22;22 Robertsonian translocation associated with recurrent abortions
M Mameli, S Cardia, A Milia, et al.
Journal of Medical Genetics
|
February 1, 1985
The prevalence of translocations in parents of children with regular trisomy 21: a possible interchromosomal effect?
R H Lindenbaum, M Hultén, A McDermott, et al.
Page
of 2