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Anticancer Research
|
April 19, 2000
I-FISH control of CGH-detected gain of DNA sequence copy number in oral squamous cell carcinomas (OSCC)
K Bayerlein, T Rith, I Verdorfer, et al.
Cytogenetic and Genome Research
|
August 8, 2013
Independent sex chromosome evolution in lower vertebrates: a molecular cytogenetic overview in the Erythrinidae fish family
M B Cioffi, T Liehr, V Trifonov, et al.
Oral Oncology
|
August 6, 1998
Oral squamous cell carcinomas are characterized by a rather uniform pattern of genomic imbalances detected by comparative genomic hybridisation
E Wolff, S Girod, T Liehr, et al.
Cytogenetics and Cell Genetics
|
November 27, 1999
Assignment of the serologically defined colon cancer antigen 1 gene (SDCCAG1) to human chromosome band 14q22 by in situ hybridization
D Carbonnelle, T Liehr, C Jacquot, et al.
Journal of Medical Genetics
|
March 8, 2003
Partial hexasomy 15pter-->15q13 including SNRPN and D15S10: first molecular cytogenetically proven case report
A Nietzel, B Albrecht, H Starke, et al.
Genomics
|
February 26, 2019
Chromosomal breakpoints in a cohort of head and neck squamous cell carcinoma patients
I P Ribeiro, I M Carreira, L Esteves, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 5, 2011
The case of an infertile male with an uncommon reciprocal X-autosomal translocation: how does this affect male fertility?
K Karaer, M A Ergun, A Weise, et al.
Clinical Genetics
|
July 16, 2003
Presumed mutation in a microsatellite marker mimicking segmental uniparental disomy in a case of a small supernumerary marker chromosome detected at prenatal diagnosis
F von Eggeling, S Langer, C Hoppe, et al.
American Journal of Medical Genetics. Part A
|
July 29, 2003
Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter --> p12.2)[10]
S Sauter, G von Beust, P Burfeind, et al.
Cytogenetic and Genome Research
|
November 12, 2003
Supernumerary small marker chromosome (SMC) and uniparental disomy 22 in a child with confined placental mosaicism of trisomy 22: trisomy rescue due to marker chromosome formation
I Bartels, G Schlueter, T Liehr, et al.
Page
of 20
Search research articles
Search
Showing results (81-90 of 192) with videos related to
Sort By:
Page
of 20
Anticancer Research
|
April 19, 2000
I-FISH control of CGH-detected gain of DNA sequence copy number in oral squamous cell carcinomas (OSCC)
K Bayerlein, T Rith, I Verdorfer, et al.
Cytogenetic and Genome Research
|
August 8, 2013
Independent sex chromosome evolution in lower vertebrates: a molecular cytogenetic overview in the Erythrinidae fish family
M B Cioffi, T Liehr, V Trifonov, et al.
Oral Oncology
|
August 6, 1998
Oral squamous cell carcinomas are characterized by a rather uniform pattern of genomic imbalances detected by comparative genomic hybridisation
E Wolff, S Girod, T Liehr, et al.
Cytogenetics and Cell Genetics
|
November 27, 1999
Assignment of the serologically defined colon cancer antigen 1 gene (SDCCAG1) to human chromosome band 14q22 by in situ hybridization
D Carbonnelle, T Liehr, C Jacquot, et al.
Journal of Medical Genetics
|
March 8, 2003
Partial hexasomy 15pter-->15q13 including SNRPN and D15S10: first molecular cytogenetically proven case report
A Nietzel, B Albrecht, H Starke, et al.
Genomics
|
February 26, 2019
Chromosomal breakpoints in a cohort of head and neck squamous cell carcinoma patients
I P Ribeiro, I M Carreira, L Esteves, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 5, 2011
The case of an infertile male with an uncommon reciprocal X-autosomal translocation: how does this affect male fertility?
K Karaer, M A Ergun, A Weise, et al.
Clinical Genetics
|
July 16, 2003
Presumed mutation in a microsatellite marker mimicking segmental uniparental disomy in a case of a small supernumerary marker chromosome detected at prenatal diagnosis
F von Eggeling, S Langer, C Hoppe, et al.
American Journal of Medical Genetics. Part A
|
July 29, 2003
Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter --> p12.2)[10]
S Sauter, G von Beust, P Burfeind, et al.
Cytogenetic and Genome Research
|
November 12, 2003
Supernumerary small marker chromosome (SMC) and uniparental disomy 22 in a child with confined placental mosaicism of trisomy 22: trisomy rescue due to marker chromosome formation
I Bartels, G Schlueter, T Liehr, et al.
Page
of 20