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International Journal of Molecular Medicine
|
April 10, 2003
Evidence for a new microdeletion syndrome in 15q21
T Liehr, H Starke, A Heller, et al.
Human Genetics
|
May 17, 2001
A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH)
A Nietzel, M Rocchi, H Starke, et al.
Clinical Genetics
|
July 16, 2003
Conspicuous GTG-banding results of the centromere-near region can be caused by alphoid DNA heteromorphism
T Liehr, M Ziegler, H Starke, et al.
Prenatal Diagnosis
|
December 18, 2001
Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB)
H Starke, G Senger, M Kossakiewicz, et al.
Journal of Medical Genetics
|
July 7, 2000
Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review
A Heller, J Seidel, A Hübler, et al.
Human Reproduction (Oxford, England)
|
February 4, 2005
Meiotic studies in two human reciprocal translocations and their association with spermatogenic failure
M Oliver-Bonet, J Benet, F Sun, et al.
Cytogenetic and Genome Research
|
September 7, 2006
De novostructural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies
A Dufke, S Singer, S Borell-Kost, et al.
Prenatal Diagnosis
|
May 22, 2001
Pitfalls of rapid prenatal diagnosis using the interphase nucleus
T Liehr, V Beensen, R Hauschild, et al.
British Journal of Haematology
|
May 31, 2001
Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative chronic myelogenous leukaemia
H Starke, M Raida, V Trifonov, et al.
Clinical Genetics
|
September 5, 2001
Tetrasomy 21 due to a de novo Robertsonian translocation t(14;21) and an additional free trisomy 21
T Liehr, V Beensen, H Starke, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 74) with videos related to
Sort By:
Page
of 8
International Journal of Molecular Medicine
|
April 10, 2003
Evidence for a new microdeletion syndrome in 15q21
T Liehr, H Starke, A Heller, et al.
Human Genetics
|
May 17, 2001
A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH)
A Nietzel, M Rocchi, H Starke, et al.
Clinical Genetics
|
July 16, 2003
Conspicuous GTG-banding results of the centromere-near region can be caused by alphoid DNA heteromorphism
T Liehr, M Ziegler, H Starke, et al.
Prenatal Diagnosis
|
December 18, 2001
Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB)
H Starke, G Senger, M Kossakiewicz, et al.
Journal of Medical Genetics
|
July 7, 2000
Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review
A Heller, J Seidel, A Hübler, et al.
Human Reproduction (Oxford, England)
|
February 4, 2005
Meiotic studies in two human reciprocal translocations and their association with spermatogenic failure
M Oliver-Bonet, J Benet, F Sun, et al.
Cytogenetic and Genome Research
|
September 7, 2006
De novostructural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies
A Dufke, S Singer, S Borell-Kost, et al.
Prenatal Diagnosis
|
May 22, 2001
Pitfalls of rapid prenatal diagnosis using the interphase nucleus
T Liehr, V Beensen, R Hauschild, et al.
British Journal of Haematology
|
May 31, 2001
Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative chronic myelogenous leukaemia
H Starke, M Raida, V Trifonov, et al.
Clinical Genetics
|
September 5, 2001
Tetrasomy 21 due to a de novo Robertsonian translocation t(14;21) and an additional free trisomy 21
T Liehr, V Beensen, H Starke, et al.
Page
of 8