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H Cleve

Showing results (91-100 of 114) with videos related to

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Human Genetics|January 1, 1984
Transferrin subtypes and variants in Germany; further evidence for a Tf null alleleS Weidinger, H Cleve, F Schwarzfischer, et al.
The Japanese Journal of Human Genetics|March 1, 1995
A novel sequence polymorphism in exon 8 of the human vitamin D-binding protein (GC) gene in an African populationI Yuasa, A Kofler, A Braun, et al.
Human Genetics|January 1, 1983
alpha 1-Antitrypsin (Pi) types and subtypes in the Tyrolean populationA Böhme, H Cleve, D Schönitzer, et al.
Journal of Immunology (Baltimore, Md. : 1950)|August 1, 1974
Immunoglobulin expression of cells from human lymphoblastoid lines. I. Heavy and light chain antigens of the cell surfaceS D Litwin, T H Hütteroth, P K Lin, et al.
American Journal of Human Genetics|March 1, 1993
True hermaphroditism in a 46,XY individual, caused by a postzygotic somatic point mutation in the male gonadal sex-determining locus (SRY): molecular genetics and histological findings in a sporadic caseA Braun, S Kammerer, H Cleve, et al.
Vox Sanguinis|January 1, 1975
ADA-7--a new alleleK Berg, H Cleve, G Hofmann, et al.
Journal of Immunology (Baltimore, Md. : 1950)|August 1, 1974
Immunoglobulin expression of cells from human lymphoblastoid lines. II. Interrelationship among surface, cellular, and secreted immunoglobulinsS D Litwin, T H Hütteroth, P K Lin, et al.
Human Genetics|July 1, 1994
The polymorphism of the plasma inter-alpha-trypsin inhibitor (ITI) and its relationship to the heavy chain H1 subunit gene (ITIH1) at 3p211-212U Vogt, R Sesboüé, J Bourguignon, et al.
Human Genetics|December 1, 1993
Familial true hermaphroditism: paternal and maternal transmission of true hermaphroditism (46,XX) and XX maleness in the absence of Y-chromosomal sequencesU Kuhnle, H P Schwarz, U Löhrs, et al.
Padiatrie Und Padologie|January 1, 1982
[Hereditary alpha 1-antitrypsin deficiency and infantile cirrhosis of the liver]S Kazda, W Müller, A Böhme, et al.
Pageof 12

Showing results (91-100 of 114) with videos related to

Sort By:
Pageof 12
Human Genetics|January 1, 1984
Transferrin subtypes and variants in Germany; further evidence for a Tf null alleleS Weidinger, H Cleve, F Schwarzfischer, et al.
The Japanese Journal of Human Genetics|March 1, 1995
A novel sequence polymorphism in exon 8 of the human vitamin D-binding protein (GC) gene in an African populationI Yuasa, A Kofler, A Braun, et al.
Human Genetics|January 1, 1983
alpha 1-Antitrypsin (Pi) types and subtypes in the Tyrolean populationA Böhme, H Cleve, D Schönitzer, et al.
Journal of Immunology (Baltimore, Md. : 1950)|August 1, 1974
Immunoglobulin expression of cells from human lymphoblastoid lines. I. Heavy and light chain antigens of the cell surfaceS D Litwin, T H Hütteroth, P K Lin, et al.
American Journal of Human Genetics|March 1, 1993
True hermaphroditism in a 46,XY individual, caused by a postzygotic somatic point mutation in the male gonadal sex-determining locus (SRY): molecular genetics and histological findings in a sporadic caseA Braun, S Kammerer, H Cleve, et al.
Vox Sanguinis|January 1, 1975
ADA-7--a new alleleK Berg, H Cleve, G Hofmann, et al.
Journal of Immunology (Baltimore, Md. : 1950)|August 1, 1974
Immunoglobulin expression of cells from human lymphoblastoid lines. II. Interrelationship among surface, cellular, and secreted immunoglobulinsS D Litwin, T H Hütteroth, P K Lin, et al.
Human Genetics|July 1, 1994
The polymorphism of the plasma inter-alpha-trypsin inhibitor (ITI) and its relationship to the heavy chain H1 subunit gene (ITIH1) at 3p211-212U Vogt, R Sesboüé, J Bourguignon, et al.
Human Genetics|December 1, 1993
Familial true hermaphroditism: paternal and maternal transmission of true hermaphroditism (46,XX) and XX maleness in the absence of Y-chromosomal sequencesU Kuhnle, H P Schwarz, U Löhrs, et al.
Padiatrie Und Padologie|January 1, 1982
[Hereditary alpha 1-antitrypsin deficiency and infantile cirrhosis of the liver]S Kazda, W Müller, A Böhme, et al.
Pageof 12