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B Zabel

Showing results (31-40 of 120) with videos related to

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Human Genetics|June 10, 1977
Short-arm deletion of an X chromosome (45,XO/46,XX p--)P Kaiser, K Gerhard-Ratschow, B Zabel, et al.
Human Genetics|November 2, 1977
A new case of XX-male (XX/XXY mosaic)P Kaiser, K Gerhard-Ratschow, B Zabel, et al.
Bone|January 1, 1990
Distribution of type I and type II collagen gene expression during the development of human long bonesS Mundlos, H Engel, I Michel-Behnke, et al.
American Journal of Medical Genetics|May 3, 1996
Osteopathia striata with cranial sclerosis: variable expressivity in a four generation pedigreeR König, C Dukiet, A Dörries, et al.
American Journal of Medical Genetics|May 3, 1996
An unknown spondylo-meta-epiphyseal dysplasia in sibs with extreme short statureH Menger, S Mundlos, K Becker, et al.
Molecular and Cellular Probes|June 1, 1996
Two different PAX3 gene mutations causing Waardenburg syndrome type IG Wildhardt, A Winterpacht, K Hilbert, et al.
European Journal of Pediatrics|January 7, 1999
Severe factor V deficiency presenting as subdural haematoma in the newbornS Ehrenforth, D Klarmann, B Zabel, et al.
European Journal of Pediatrics|July 1, 1995
Nephropathy with Wilms tumour or gonadal dysgenesis: incomplete Denys-Drash syndrome or separate diseases?K Schmitt, B Zabel, G Tulzer, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Human CLAPS2 encoding AP17, a small chain of the clathrin-associated protein complex: cDNA cloning and chromosomal assignment to 19q13.2-->q13.3A Winterpacht, S Endele, T Enklaar, et al.
Deutsche Medizinische Wochenschrift (1946)|July 2, 1982
[Improvement in the longitudinal growth in Ullrich-Turner syndrome with oxandrolone. Function of urinary excretion of steroid hormones]W Schönberger, P Benes, B Morsches, et al.
Pageof 12

Showing results (31-40 of 120) with videos related to

Sort By:
Pageof 12
Human Genetics|June 10, 1977
Short-arm deletion of an X chromosome (45,XO/46,XX p--)P Kaiser, K Gerhard-Ratschow, B Zabel, et al.
Human Genetics|November 2, 1977
A new case of XX-male (XX/XXY mosaic)P Kaiser, K Gerhard-Ratschow, B Zabel, et al.
Bone|January 1, 1990
Distribution of type I and type II collagen gene expression during the development of human long bonesS Mundlos, H Engel, I Michel-Behnke, et al.
American Journal of Medical Genetics|May 3, 1996
Osteopathia striata with cranial sclerosis: variable expressivity in a four generation pedigreeR König, C Dukiet, A Dörries, et al.
American Journal of Medical Genetics|May 3, 1996
An unknown spondylo-meta-epiphyseal dysplasia in sibs with extreme short statureH Menger, S Mundlos, K Becker, et al.
Molecular and Cellular Probes|June 1, 1996
Two different PAX3 gene mutations causing Waardenburg syndrome type IG Wildhardt, A Winterpacht, K Hilbert, et al.
European Journal of Pediatrics|January 7, 1999
Severe factor V deficiency presenting as subdural haematoma in the newbornS Ehrenforth, D Klarmann, B Zabel, et al.
European Journal of Pediatrics|July 1, 1995
Nephropathy with Wilms tumour or gonadal dysgenesis: incomplete Denys-Drash syndrome or separate diseases?K Schmitt, B Zabel, G Tulzer, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Human CLAPS2 encoding AP17, a small chain of the clathrin-associated protein complex: cDNA cloning and chromosomal assignment to 19q13.2-->q13.3A Winterpacht, S Endele, T Enklaar, et al.
Deutsche Medizinische Wochenschrift (1946)|July 2, 1982
[Improvement in the longitudinal growth in Ullrich-Turner syndrome with oxandrolone. Function of urinary excretion of steroid hormones]W Schönberger, P Benes, B Morsches, et al.
Pageof 12