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Human Genetics
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September 1, 1997
Localization of the gene for Wieacker-Wolff syndrome in the pericentromeric region of the X chromosome
D U Kloos, S Jakubiczka, T Wienker, et al.
Cancer Genetics and Cytogenetics
|
May 17, 2000
A novel translocation (17;19)(p13;p13) in a patient with acute myelomonocytic leukemia
R Brückner, K Jentsch-Ullrich, A Franke, et al.
Cytogenetics and Cell Genetics
|
February 22, 2002
Expression pattern and further characterization of human MAGED2 and identification of rodent orthologues
K Langnaese, D U Kloos, M Wehnert, et al.
Annals of Hematology
|
March 21, 2002
High reliability and sensitivity of the BCR/ABL1 D-FISH test for the detection of BCR/ABL rearrangements
A F Pelz, H Kröning, A Franke, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)
|
August 1, 1992
[The normal vascularization of the female breast in Doppler ultrasound]
H Madjar, M Vetter, H J Prömpeler, et al.
Zentralblatt Fur Gynakologie
|
January 9, 1999
[XY gonadal dysgenesis (Swyer syndrome) with gonadoblastoma]
A Lange, P Wieacker, R Schnabel, et al.
Geburtshilfe Und Frauenheilkunde
|
September 1, 1990
[Prognosis of triplet pregnancies]
H J Prömpeler, C Wilhelm, H Madjar, et al.
Clinical Dysmorphology
|
July 12, 2001
Campomelic dysplasia without sex reversal in a Turkish patient is due to mutation Ala119Val within the SOX9 gene
S Jakubiczka, T Bettecken, G Koch, et al.
Neuropediatrics
|
August 23, 2007
Congenital cataract, ataxia, external ophthalmoplegia and dysphagia in two siblings. A Marinesco-Sjögren-like syndrome
S Schulz, S Vielhaber, P Muschke, et al.
Geburtshilfe Und Frauenheilkunde
|
November 1, 1988
[Effect of sex steroids on the lipoprotein profile]
H J Prömpeler, J Neulen, P Wieacker, et al.
Page
of 11
Search research articles
Search
Showing results (51-60 of 105) with videos related to
Sort By:
Page
of 11
Human Genetics
|
September 1, 1997
Localization of the gene for Wieacker-Wolff syndrome in the pericentromeric region of the X chromosome
D U Kloos, S Jakubiczka, T Wienker, et al.
Cancer Genetics and Cytogenetics
|
May 17, 2000
A novel translocation (17;19)(p13;p13) in a patient with acute myelomonocytic leukemia
R Brückner, K Jentsch-Ullrich, A Franke, et al.
Cytogenetics and Cell Genetics
|
February 22, 2002
Expression pattern and further characterization of human MAGED2 and identification of rodent orthologues
K Langnaese, D U Kloos, M Wehnert, et al.
Annals of Hematology
|
March 21, 2002
High reliability and sensitivity of the BCR/ABL1 D-FISH test for the detection of BCR/ABL rearrangements
A F Pelz, H Kröning, A Franke, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)
|
August 1, 1992
[The normal vascularization of the female breast in Doppler ultrasound]
H Madjar, M Vetter, H J Prömpeler, et al.
Zentralblatt Fur Gynakologie
|
January 9, 1999
[XY gonadal dysgenesis (Swyer syndrome) with gonadoblastoma]
A Lange, P Wieacker, R Schnabel, et al.
Geburtshilfe Und Frauenheilkunde
|
September 1, 1990
[Prognosis of triplet pregnancies]
H J Prömpeler, C Wilhelm, H Madjar, et al.
Clinical Dysmorphology
|
July 12, 2001
Campomelic dysplasia without sex reversal in a Turkish patient is due to mutation Ala119Val within the SOX9 gene
S Jakubiczka, T Bettecken, G Koch, et al.
Neuropediatrics
|
August 23, 2007
Congenital cataract, ataxia, external ophthalmoplegia and dysphagia in two siblings. A Marinesco-Sjögren-like syndrome
S Schulz, S Vielhaber, P Muschke, et al.
Geburtshilfe Und Frauenheilkunde
|
November 1, 1988
[Effect of sex steroids on the lipoprotein profile]
H J Prömpeler, J Neulen, P Wieacker, et al.
Page
of 11