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Human Genetics
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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 bones
S 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 pedigree
R 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 stature
H Menger, S Mundlos, K Becker, et al.
Molecular and Cellular Probes
|
June 1, 1996
Two different PAX3 gene mutations causing Waardenburg syndrome type I
G Wildhardt, A Winterpacht, K Hilbert, et al.
European Journal of Pediatrics
|
January 7, 1999
Severe factor V deficiency presenting as subdural haematoma in the newborn
S 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-->q13.3
A 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.
Page
of 12
Search research articles
Search
Showing results (31-40 of 120) with videos related to
Sort By:
Page
of 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 bones
S 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 pedigree
R 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 stature
H Menger, S Mundlos, K Becker, et al.
Molecular and Cellular Probes
|
June 1, 1996
Two different PAX3 gene mutations causing Waardenburg syndrome type I
G Wildhardt, A Winterpacht, K Hilbert, et al.
European Journal of Pediatrics
|
January 7, 1999
Severe factor V deficiency presenting as subdural haematoma in the newborn
S 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-->q13.3
A 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.
Page
of 12