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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.
Gene
|
December 17, 2013
A patient with partial trisomy 21 and 7q deletion expresses mild Down syndrome phenotype
I Papoulidis, E Papageorgiou, E Siomou, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association
|
March 28, 2003
Putative colon cancer risk factors damage global DNA and TP53 in primary human colon cells isolated from surgical samples
A Schaeferhenrich, W Sendt, J Scheele, 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.
Hamostaseologie
|
November 6, 2015
Large deletions play a minor but essential role in congenital coagulation factor VII and X deficiencies
M Rath, J Najm, H Sirb, et al.
American Journal of Medical Genetics. Part A
|
September 4, 2010
Characterization of a complex cryptic mosaicism for an sSMC derived from the X chromosome present in a boy with congenital malformations
M Santos, K Mrasek, I Madrigal, 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.
Molecular Cytogenetics
|
August 4, 2016
Partial monosomy14q involving FOXG1 and NOVA1 in an infant with microcephaly, seizures and severe developmental delay
H Fryssira, E Tsoutsou, S Psoni, 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.
Page
of 20
Search research articles
Search
Showing results (141-150 of 192) with videos related to
Sort By:
Page
of 20
International Journal of Molecular Medicine
|
April 10, 2003
Evidence for a new microdeletion syndrome in 15q21
T Liehr, H Starke, A Heller, et al.
Gene
|
December 17, 2013
A patient with partial trisomy 21 and 7q deletion expresses mild Down syndrome phenotype
I Papoulidis, E Papageorgiou, E Siomou, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association
|
March 28, 2003
Putative colon cancer risk factors damage global DNA and TP53 in primary human colon cells isolated from surgical samples
A Schaeferhenrich, W Sendt, J Scheele, 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.
Hamostaseologie
|
November 6, 2015
Large deletions play a minor but essential role in congenital coagulation factor VII and X deficiencies
M Rath, J Najm, H Sirb, et al.
American Journal of Medical Genetics. Part A
|
September 4, 2010
Characterization of a complex cryptic mosaicism for an sSMC derived from the X chromosome present in a boy with congenital malformations
M Santos, K Mrasek, I Madrigal, 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.
Molecular Cytogenetics
|
August 4, 2016
Partial monosomy14q involving FOXG1 and NOVA1 in an infant with microcephaly, seizures and severe developmental delay
H Fryssira, E Tsoutsou, S Psoni, 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.
Page
of 20