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M E Ferguson-Smith

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Prenatal Diagnosis|November 1, 1994
Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: a prospective studyD H Spathas, A Divane, G M Maniatis, et al.
Cytometry|January 1, 1990
Study of X chromosome abnormality in XX males using bivariate flow karyotype analysis and flow sorted dot blotsN P Carter, M E Ferguson-Smith, N A Affara, et al.
Human Genetics|October 1, 1988
Siblings with chromosome mosaicism, microcephaly, and growth retardation: the phenotypic expression of a human mitotic mutant?J L Tolmie, E Boyd, P Batstone, et al.
Journal of Medical Genetics|February 1, 1986
Early prenatal investigation of a pregnancy at risk of adenosine deaminase deficiency using chorionic villiD A Aitken, D H Gilmore, C A Frew, et al.
Lancet (London, England)|May 5, 1973
Antenatal diagnosis of propianicacidaemiaD Gompertz, P A Goodey, H Thom, et al.
Prenatal Diagnosis|November 1, 1992
Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridization using a cosmid contigY L Zheng, M A Ferguson-Smith, J P Warner, et al.
Journal of Medical Genetics|October 1, 1992
A male with trisomy 9 mosaicism and maternal uniparental disomy for chromosome 9 in the euploid cell lineL R Willatt, B C Davison, D Goudie, et al.
Prenatal Diagnosis|May 1, 1994
Second-trimester maternal serum screening using alpha-fetoprotein, human chorionic gonadotrophin, and unconjugated oestriol: experience of a regional programmeS F Goodburn, J R Yates, P R Raggatt, et al.
Clinical Genetics|October 1, 1975
Prenatal diagnosis and family studies in a case of propionicacidaemiaD Gompertz, P A Goodey, H Thom, et al.
Human Genetics|August 1, 1993
Physical mapping of chromosome 3p25-p26 by fluorescence in situ hybridisation (FISH)M E Phipps, E R Maher, N A Affara, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Prenatal Diagnosis|November 1, 1994
Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: a prospective studyD H Spathas, A Divane, G M Maniatis, et al.
Cytometry|January 1, 1990
Study of X chromosome abnormality in XX males using bivariate flow karyotype analysis and flow sorted dot blotsN P Carter, M E Ferguson-Smith, N A Affara, et al.
Human Genetics|October 1, 1988
Siblings with chromosome mosaicism, microcephaly, and growth retardation: the phenotypic expression of a human mitotic mutant?J L Tolmie, E Boyd, P Batstone, et al.
Journal of Medical Genetics|February 1, 1986
Early prenatal investigation of a pregnancy at risk of adenosine deaminase deficiency using chorionic villiD A Aitken, D H Gilmore, C A Frew, et al.
Lancet (London, England)|May 5, 1973
Antenatal diagnosis of propianicacidaemiaD Gompertz, P A Goodey, H Thom, et al.
Prenatal Diagnosis|November 1, 1992
Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridization using a cosmid contigY L Zheng, M A Ferguson-Smith, J P Warner, et al.
Journal of Medical Genetics|October 1, 1992
A male with trisomy 9 mosaicism and maternal uniparental disomy for chromosome 9 in the euploid cell lineL R Willatt, B C Davison, D Goudie, et al.
Prenatal Diagnosis|May 1, 1994
Second-trimester maternal serum screening using alpha-fetoprotein, human chorionic gonadotrophin, and unconjugated oestriol: experience of a regional programmeS F Goodburn, J R Yates, P R Raggatt, et al.
Clinical Genetics|October 1, 1975
Prenatal diagnosis and family studies in a case of propionicacidaemiaD Gompertz, P A Goodey, H Thom, et al.
Human Genetics|August 1, 1993
Physical mapping of chromosome 3p25-p26 by fluorescence in situ hybridisation (FISH)M E Phipps, E R Maher, N A Affara, et al.
Pageof 2