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J C Llerena

Showing results (1-10 of 36) with videos related to

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American Journal of Medical Genetics|January 31, 1998
Regarding the Smith-Magenis syndrome multidisciplinary clinical study by Greenberg et al [1996]J C Llerena
Human Genetics|December 1, 1988
A mosaic 45,X/46,X,r(?) karyotype investigated with X and Y centromere-specific probes using a non-autoradiographic in situ hybridization techniqueJ A Crolla, J C Llerena
Seminars in Hematology|April 11, 1991
Bloom syndrome and ataxia telangiectasiaJ C Llerena, M Murer-Orlando
American Journal of Medical Genetics|August 1, 1993
Peters' plus syndromeJ C de Almeida, J C Llerena Júnior
International Journal of Molecular Medicine|December 22, 1999
FRAXE mutation in mentally retarded patients using the OxE18 probeM V Mulatinho, J C Llerena, M M Pimentel
Genetic Testing|January 6, 2001
FRAXA screening in Brazilian institutionalized individuals with nonspecific severe mental retardationM V Mulatinho, J C Llerena, M M Pimentel
Annales De Genetique|January 1, 1991
Pure 4p trisomy due to a de novo 4q;22p dicentric translocated chromosome karyotype 46,XX,-22,+t(4;22)(q1200;p13)J C de Almeida, D F Reis, J C Llerena Júnior
Journal of Medical Genetics|July 1, 1993
Cystic fibrosis and deafnessJ C Llerena Júnior, W Degrave, A De Miranda, et al.
Folia Primatologica; International Journal of Primatology|January 1, 1995
Cytogenetic study in a specimen of Cebus apella with an atypical phenotypeB Goldschmidt, M A Airosa Cabrera, M Weinzetl, et al.
Annales De Genetique|January 1, 1989
"Pure" partial trisomy 3p due to the malsegregation of a balanced maternal translocation t (X;3) (p22.3;p21)J C de Almeida, D F Reis, J C Llerena, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|January 31, 1998
Regarding the Smith-Magenis syndrome multidisciplinary clinical study by Greenberg et al [1996]J C Llerena
Human Genetics|December 1, 1988
A mosaic 45,X/46,X,r(?) karyotype investigated with X and Y centromere-specific probes using a non-autoradiographic in situ hybridization techniqueJ A Crolla, J C Llerena
Seminars in Hematology|April 11, 1991
Bloom syndrome and ataxia telangiectasiaJ C Llerena, M Murer-Orlando
American Journal of Medical Genetics|August 1, 1993
Peters' plus syndromeJ C de Almeida, J C Llerena Júnior
International Journal of Molecular Medicine|December 22, 1999
FRAXE mutation in mentally retarded patients using the OxE18 probeM V Mulatinho, J C Llerena, M M Pimentel
Genetic Testing|January 6, 2001
FRAXA screening in Brazilian institutionalized individuals with nonspecific severe mental retardationM V Mulatinho, J C Llerena, M M Pimentel
Annales De Genetique|January 1, 1991
Pure 4p trisomy due to a de novo 4q;22p dicentric translocated chromosome karyotype 46,XX,-22,+t(4;22)(q1200;p13)J C de Almeida, D F Reis, J C Llerena Júnior
Journal of Medical Genetics|July 1, 1993
Cystic fibrosis and deafnessJ C Llerena Júnior, W Degrave, A De Miranda, et al.
Folia Primatologica; International Journal of Primatology|January 1, 1995
Cytogenetic study in a specimen of Cebus apella with an atypical phenotypeB Goldschmidt, M A Airosa Cabrera, M Weinzetl, et al.
Annales De Genetique|January 1, 1989
"Pure" partial trisomy 3p due to the malsegregation of a balanced maternal translocation t (X;3) (p22.3;p21)J C de Almeida, D F Reis, J C Llerena, et al.
Pageof 4