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Acta Physiologica (Oxford, England)
|
August 4, 2015
Mouse white adipose tissue-derived mesenchymal stem cells gain pericentral and periportal hepatocyte features after differentiation in vitro, which are preserved in vivo after hepatic transplantation
S Winkler, M Hempel, S Brückner, et al.
Journal of Medical Genetics
|
July 13, 2002
Maternal uniparental disomy 12 in a healthy girl with a 47,XX,+der(12)(:p11-->q11:)/46,XX karyotype
F Von Eggeling, C Hoppe, U Bartz, et al.
Cytogenetic and Genome Research
|
February 14, 2003
A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis
R Trappe, D Böhm, J Kohlhase, et al.
International Journal of Molecular Medicine
|
May 15, 2001
A long distance-PCR derived FISH probe detects a deletion between p15 and p16 in CML and T-ALL patients
A Bleichert, W Fiedler, U Claussen, et al.
Cytogenetic and Genome Research
|
January 9, 2013
Clinical impact of somatic mosaicism in cases with small supernumerary marker chromosomes
T Liehr, E Klein, K Mrasek, et al.
Cytogenetic and Genome Research
|
October 19, 2013
Branchio-otic syndrome caused by a genomic rearrangement: clinical findings and molecular cytogenetic studies in a patient with a pericentric inversion of chromosome 8
T Schmidt, T Bierhals, F Kortüm, et al.
Molecular Human Reproduction
|
October 5, 2007
Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm
S Bhatt, K Moradkhani, K Mrasek, et al.
International Journal of Molecular Medicine
|
December 16, 1998
Mosaicism for Charcot-Marie-Tooth disease type 1A: onset in childhood suggests somatic reversion in early developmental stages
B Rautenstrauss, T Liehr, C Fuchs, et al.
Genomics
|
May 20, 1999
Regional localization of the human epithelial membrane protein genes 1, 2, and 3 (EMP1, EMP2, EMP3) to 12p12.3, 16p13.2, and 19q13.3
T Liehr, G Kuhlenbäumer, P Wulf, et al.
Journal of Medical Genetics
|
June 19, 2002
Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes
A Weise, H Starke, A Heller, et al.
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Search research articles
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Showing results (131-140 of 192) with videos related to
Sort By:
Page
of 20
Acta Physiologica (Oxford, England)
|
August 4, 2015
Mouse white adipose tissue-derived mesenchymal stem cells gain pericentral and periportal hepatocyte features after differentiation in vitro, which are preserved in vivo after hepatic transplantation
S Winkler, M Hempel, S Brückner, et al.
Journal of Medical Genetics
|
July 13, 2002
Maternal uniparental disomy 12 in a healthy girl with a 47,XX,+der(12)(:p11-->q11:)/46,XX karyotype
F Von Eggeling, C Hoppe, U Bartz, et al.
Cytogenetic and Genome Research
|
February 14, 2003
A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis
R Trappe, D Böhm, J Kohlhase, et al.
International Journal of Molecular Medicine
|
May 15, 2001
A long distance-PCR derived FISH probe detects a deletion between p15 and p16 in CML and T-ALL patients
A Bleichert, W Fiedler, U Claussen, et al.
Cytogenetic and Genome Research
|
January 9, 2013
Clinical impact of somatic mosaicism in cases with small supernumerary marker chromosomes
T Liehr, E Klein, K Mrasek, et al.
Cytogenetic and Genome Research
|
October 19, 2013
Branchio-otic syndrome caused by a genomic rearrangement: clinical findings and molecular cytogenetic studies in a patient with a pericentric inversion of chromosome 8
T Schmidt, T Bierhals, F Kortüm, et al.
Molecular Human Reproduction
|
October 5, 2007
Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm
S Bhatt, K Moradkhani, K Mrasek, et al.
International Journal of Molecular Medicine
|
December 16, 1998
Mosaicism for Charcot-Marie-Tooth disease type 1A: onset in childhood suggests somatic reversion in early developmental stages
B Rautenstrauss, T Liehr, C Fuchs, et al.
Genomics
|
May 20, 1999
Regional localization of the human epithelial membrane protein genes 1, 2, and 3 (EMP1, EMP2, EMP3) to 12p12.3, 16p13.2, and 19q13.3
T Liehr, G Kuhlenbäumer, P Wulf, et al.
Journal of Medical Genetics
|
June 19, 2002
Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes
A Weise, H Starke, A Heller, et al.
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of 20