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A Smith

Clinical genetics

Showing results (1-10 of 16) with videos related to

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Clinical Genetics|May 1, 1980
Occurrence of sex chromosome mosaicism and translocation Down's syndrome in the same familyA Smith, G Elliott
Clinical Genetics|October 1, 1993
Alternate, adjacent 2 and 3:1 meiotic segregation products from a balanced t(13;18) (q12;q11) carrierC Cotton, M Cummins, A Smith
Clinical Genetics|June 18, 1998
Normal growth in Angelman syndrome due to paternal UPDA Smith, L Robson, B Buchholz
Clinical Genetics|July 1, 1983
Chromosome aneuploidy in Alzheimer's diseaseA Smith, G A Broe, M Williamson
Clinical Genetics|May 1, 1984
Chromosome fragility in Alzheimer's diseaseA Smith, G A Broe, M Williamson
Clinical Genetics|September 1, 1979
Translocation 46XY, t (17;18) (q25;q21) in a mentally retarded boy with progressive eye abnormalitiesA Smith, V Caradus, J G Henry
Clinical Genetics|February 27, 2013
Doing the right thing for one's children: deciding whether to take the genetic test for Huntington's disease as a moral dilemmaJ A Smith, M Stephenson, C Jacobs, et al.
Clinical Genetics|June 1, 1986
Xp21/autosome translocations. Case report and risk for Duchenne muscular dystrophyJ J Holden, A Smith, P M MacLeod, et al.
Clinical Genetics|June 1, 1990
Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNAM Upadhyaya, R A Smith, N S Thomas, et al.
Clinical Genetics|January 1, 1993
Fluorescence in-situ hybridisation and molecular studies used in the characterisation of a Robertsonian translocation (13q15q) in Prader-Willi syndromeA Smith, L Robson, A Neumann, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Clinical Genetics|May 1, 1980
Occurrence of sex chromosome mosaicism and translocation Down's syndrome in the same familyA Smith, G Elliott
Clinical Genetics|October 1, 1993
Alternate, adjacent 2 and 3:1 meiotic segregation products from a balanced t(13;18) (q12;q11) carrierC Cotton, M Cummins, A Smith
Clinical Genetics|June 18, 1998
Normal growth in Angelman syndrome due to paternal UPDA Smith, L Robson, B Buchholz
Clinical Genetics|July 1, 1983
Chromosome aneuploidy in Alzheimer's diseaseA Smith, G A Broe, M Williamson
Clinical Genetics|May 1, 1984
Chromosome fragility in Alzheimer's diseaseA Smith, G A Broe, M Williamson
Clinical Genetics|September 1, 1979
Translocation 46XY, t (17;18) (q25;q21) in a mentally retarded boy with progressive eye abnormalitiesA Smith, V Caradus, J G Henry
Clinical Genetics|February 27, 2013
Doing the right thing for one's children: deciding whether to take the genetic test for Huntington's disease as a moral dilemmaJ A Smith, M Stephenson, C Jacobs, et al.
Clinical Genetics|June 1, 1986
Xp21/autosome translocations. Case report and risk for Duchenne muscular dystrophyJ J Holden, A Smith, P M MacLeod, et al.
Clinical Genetics|June 1, 1990
Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNAM Upadhyaya, R A Smith, N S Thomas, et al.
Clinical Genetics|January 1, 1993
Fluorescence in-situ hybridisation and molecular studies used in the characterisation of a Robertsonian translocation (13q15q) in Prader-Willi syndromeA Smith, L Robson, A Neumann, et al.
Pageof 2