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Human Genetics
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February 1, 1991
No evidence for sequences structurally related to the RB1 gene in the human genome
C Belka, V Greger, B Zabel, et al.
Die Medizinische Welt
|
June 26, 1981
[Klinefelter syndrome - an unusual occurrence. Observations on 59 patients]
U Theile, J Oepen, U Cordes, et al.
Genomics
|
June 1, 1994
WT1 mutations associated with incomplete Denys-Drash syndrome define a domain predicted to behave in a dominant-negative fashion
N Bardeesy, B Zabel, K Schmitt, et al.
Human Genetics
|
April 1, 1995
Non-radioactive multiplex-SSCP analysis: detection of a new type II procollagen gene (COL2A1) mutation
A Winterpacht, K Hilbert, U Schwarze, et al.
Human Genetics
|
August 1, 1997
Human fibroblast growth factor receptor 3 gene (FGFR3): genomic sequence and primer set information for gene analysis
C Wüchner, K Hilbert, B Zabel, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
April 1, 1991
[Hepatitis B virus DNA. Current diagnosis in children with chronic hepatitis B]
S Wirth, K M Keller, W Baumann, et al.
Mechanisms of Development
|
March 12, 1999
Regulation of chondrocyte differentiation by Cbfa1
I S Kim, F Otto, B Zabel, et al.
Genomics
|
March 10, 2000
Mapping and structure of DMXL1, a human homologue of the DmX gene from Drosophila melanogaster coding for a WD repeat protein
C Kraemer, T Enklaar, B Zabel, et al.
Human Genetics
|
April 7, 1977
A girl with partial long-arm deletion of chromosome 11 and familial pericentric inversion of chromosome 9
B Zabel, S Hansen, U Hilig, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
May 1, 1992
Hepatitis B virus DNA in liver tissue of chronic HBsAg carriers in childhood and its relationship to other viral markers
S Wirth, K M Keller, E Schaefer, et al.
Page
of 12
Search research articles
Search
Showing results (21-30 of 120) with videos related to
Sort By:
Page
of 12
Human Genetics
|
February 1, 1991
No evidence for sequences structurally related to the RB1 gene in the human genome
C Belka, V Greger, B Zabel, et al.
Die Medizinische Welt
|
June 26, 1981
[Klinefelter syndrome - an unusual occurrence. Observations on 59 patients]
U Theile, J Oepen, U Cordes, et al.
Genomics
|
June 1, 1994
WT1 mutations associated with incomplete Denys-Drash syndrome define a domain predicted to behave in a dominant-negative fashion
N Bardeesy, B Zabel, K Schmitt, et al.
Human Genetics
|
April 1, 1995
Non-radioactive multiplex-SSCP analysis: detection of a new type II procollagen gene (COL2A1) mutation
A Winterpacht, K Hilbert, U Schwarze, et al.
Human Genetics
|
August 1, 1997
Human fibroblast growth factor receptor 3 gene (FGFR3): genomic sequence and primer set information for gene analysis
C Wüchner, K Hilbert, B Zabel, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
April 1, 1991
[Hepatitis B virus DNA. Current diagnosis in children with chronic hepatitis B]
S Wirth, K M Keller, W Baumann, et al.
Mechanisms of Development
|
March 12, 1999
Regulation of chondrocyte differentiation by Cbfa1
I S Kim, F Otto, B Zabel, et al.
Genomics
|
March 10, 2000
Mapping and structure of DMXL1, a human homologue of the DmX gene from Drosophila melanogaster coding for a WD repeat protein
C Kraemer, T Enklaar, B Zabel, et al.
Human Genetics
|
April 7, 1977
A girl with partial long-arm deletion of chromosome 11 and familial pericentric inversion of chromosome 9
B Zabel, S Hansen, U Hilig, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
May 1, 1992
Hepatitis B virus DNA in liver tissue of chronic HBsAg carriers in childhood and its relationship to other viral markers
S Wirth, K M Keller, E Schaefer, et al.
Page
of 12