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J J Waters

Showing results (11-20 of 23) with videos related to

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American Journal of Medical Genetics|July 1, 1990
Trisomy 20q caused by der (X)t(X;20)(q28;q11.2)J J Waters, D S Gourley, D A Aitken, et al.
Journal of Medical Genetics|September 1, 1991
Chromosome in situ suppression hybridisation in clinical cytogeneticsM A Hulten, C P Gould, A S Goldman, et al.
Placenta|July 1, 1982
The protein composition of the fibrinoid material at the human uteroplacental interfaceR G Sutcliffe, M Davies, J B Hunter, et al.
Journal of Cellular Biochemistry|April 1, 1987
Oncogene amplification and chromosomal abnormalities in small cell lung cancerJ M Ibson, J J Waters, P R Twentyman, et al.
Cancer Genetics and Cytogenetics|February 1, 1988
Cytogenetic abnormalities in human small cell lung carcinoma: cell lines characterized for myc gene amplificationJ J Waters, J M Ibson, P R Twentyman, et al.
Prenatal Diagnosis|October 1, 1990
Prenatal diagnosis of a double bisatellited marker with an unusual copy number ratioJ J Waters, M E Ferguson-Smith, N Carter, et al.
Lancet (London, England)|August 22, 1992
Rapid interphase FISH diagnosis of trisomy 18 on blood smearsC M McKeown, J J Waters, M Stacey, et al.
The EMBO Journal|February 1, 1988
The mechanism of chromosomal translocation t(11;14) involving the T-cell receptor C delta locus on human chromosome 14q11 and a transcribed region of chromosome 11p15T Boehm, R Baer, I Lavenir, et al.
Journal of Clinical Pathology|August 1, 1996
Solid tissue culture for cytogenetic analysis: a collaborative survey for the Association of Clinical CytogeneticistsC S Rodgers, M R Creasy, M Fitchett, et al.
British Journal of Haematology|April 7, 1999
The sequential analysis of trisomy 12 in B-cell chronic lymphocytic leukaemiaR L Auer, N Bienz, J Neilson, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|July 1, 1990
Trisomy 20q caused by der (X)t(X;20)(q28;q11.2)J J Waters, D S Gourley, D A Aitken, et al.
Journal of Medical Genetics|September 1, 1991
Chromosome in situ suppression hybridisation in clinical cytogeneticsM A Hulten, C P Gould, A S Goldman, et al.
Placenta|July 1, 1982
The protein composition of the fibrinoid material at the human uteroplacental interfaceR G Sutcliffe, M Davies, J B Hunter, et al.
Journal of Cellular Biochemistry|April 1, 1987
Oncogene amplification and chromosomal abnormalities in small cell lung cancerJ M Ibson, J J Waters, P R Twentyman, et al.
Cancer Genetics and Cytogenetics|February 1, 1988
Cytogenetic abnormalities in human small cell lung carcinoma: cell lines characterized for myc gene amplificationJ J Waters, J M Ibson, P R Twentyman, et al.
Prenatal Diagnosis|October 1, 1990
Prenatal diagnosis of a double bisatellited marker with an unusual copy number ratioJ J Waters, M E Ferguson-Smith, N Carter, et al.
Lancet (London, England)|August 22, 1992
Rapid interphase FISH diagnosis of trisomy 18 on blood smearsC M McKeown, J J Waters, M Stacey, et al.
The EMBO Journal|February 1, 1988
The mechanism of chromosomal translocation t(11;14) involving the T-cell receptor C delta locus on human chromosome 14q11 and a transcribed region of chromosome 11p15T Boehm, R Baer, I Lavenir, et al.
Journal of Clinical Pathology|August 1, 1996
Solid tissue culture for cytogenetic analysis: a collaborative survey for the Association of Clinical CytogeneticistsC S Rodgers, M R Creasy, M Fitchett, et al.
British Journal of Haematology|April 7, 1999
The sequential analysis of trisomy 12 in B-cell chronic lymphocytic leukaemiaR L Auer, N Bienz, J Neilson, et al.
Pageof 3