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T O Goecke

Showing results (1-10 of 11) with videos related to

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American Journal of Medical Genetics|November 4, 1998
Microcephalic osteodysplastic primordial dwarfism type II: report of three cases and reviewF Majewski, T O Goecke
Anthropologischer Anzeiger; Bericht Uber Die Biologisch-Anthropologische Literatur|December 1, 1984
[Head measurements and body height in 18 to 20-year-old males in a West German population (Dusseldorf district)]H G Scheil, T O Goecke
Anthropologischer Anzeiger; Bericht Uber Die Biologisch-Anthropologische Literatur|March 1, 1987
[Anthropometric studies of a student sample of Düsseldorf University]G Frahsek, H G Scheil, T O Goecke
Anthropologischer Anzeiger; Bericht Uber Die Biologisch-Anthropologische Literatur|March 1, 1988
[The problem of "benign macrocephaly"]G Frahsek, T O Goecke, H G Scheil
European Journal of Cancer Prevention : the Official Journal of the European Cancer Prevention Organisation (ECP)|August 23, 2000
Prevention and therapy for BRCA1/2 mutation carriers and women at high risk for breast and ovarian cancerB Kuschel, M P Lux, T O Goecke, et al.
Clinical Genetics|March 23, 2004
SDHD mutation analysis in seven German patients with sporadic carotid body paraganglioma: one novel mutation, no Dutch founder mutation and further evidence that G12S is a polymorphismB Leube, R Huber, T O Goecke, et al.
Brain & Development|March 1, 1995
Prenatal diagnosis of infantile neuronal ceroid-lipofuscinosis: a combined electron microscopic and molecular genetic approachH H Goebel, J Vesa, B Reitter, et al.
Praxis|June 3, 1998
[Tumor risk consultation for predisposed women from high risk cancer families]M W Beckmann, D Niederacher, R Bodden-Heidrich, et al.
European Journal of Cancer Prevention : the Official Journal of the European Cancer Prevention Organisation (ECP)|July 21, 2005
Use of intensified early cancer detection in high-risk patients with familial breast and ovarian cancerM P Lux, S Ackermann, C Nestle-Krämling, et al.
American Journal of Human Genetics|August 2, 2007
A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGINK Lehmann, P Seemann, F Silan, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics|November 4, 1998
Microcephalic osteodysplastic primordial dwarfism type II: report of three cases and reviewF Majewski, T O Goecke
Anthropologischer Anzeiger; Bericht Uber Die Biologisch-Anthropologische Literatur|December 1, 1984
[Head measurements and body height in 18 to 20-year-old males in a West German population (Dusseldorf district)]H G Scheil, T O Goecke
Anthropologischer Anzeiger; Bericht Uber Die Biologisch-Anthropologische Literatur|March 1, 1987
[Anthropometric studies of a student sample of Düsseldorf University]G Frahsek, H G Scheil, T O Goecke
Anthropologischer Anzeiger; Bericht Uber Die Biologisch-Anthropologische Literatur|March 1, 1988
[The problem of "benign macrocephaly"]G Frahsek, T O Goecke, H G Scheil
European Journal of Cancer Prevention : the Official Journal of the European Cancer Prevention Organisation (ECP)|August 23, 2000
Prevention and therapy for BRCA1/2 mutation carriers and women at high risk for breast and ovarian cancerB Kuschel, M P Lux, T O Goecke, et al.
Clinical Genetics|March 23, 2004
SDHD mutation analysis in seven German patients with sporadic carotid body paraganglioma: one novel mutation, no Dutch founder mutation and further evidence that G12S is a polymorphismB Leube, R Huber, T O Goecke, et al.
Brain & Development|March 1, 1995
Prenatal diagnosis of infantile neuronal ceroid-lipofuscinosis: a combined electron microscopic and molecular genetic approachH H Goebel, J Vesa, B Reitter, et al.
Praxis|June 3, 1998
[Tumor risk consultation for predisposed women from high risk cancer families]M W Beckmann, D Niederacher, R Bodden-Heidrich, et al.
European Journal of Cancer Prevention : the Official Journal of the European Cancer Prevention Organisation (ECP)|July 21, 2005
Use of intensified early cancer detection in high-risk patients with familial breast and ovarian cancerM P Lux, S Ackermann, C Nestle-Krämling, et al.
American Journal of Human Genetics|August 2, 2007
A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGINK Lehmann, P Seemann, F Silan, et al.
Pageof 2