Add to ORKGZymed’s SPzT-Light ® Chromosome 19q Probe is intended to detect the number of chromosome 19q in formalin-fixed, paraffin-embedded (FFPE) tissue sections using Chromogenic In Situ Hybridization (CISH™). Interpretation must be made within the context of the patient’s clinical history by a qualified pathologist
Structural rearrangements involving the long arm of chromosome 19 characterize a cytogenetic subgrou...
In this study of ovarian carcinoma, we extended previous findings by performing FISH using chromosom...
The 1p/19q codeletion is the result of a translocation between chromosome 1 (Chr1p) and chromosome 1...
We report here the band location of 540 cosmids mapped to chromosome 19. The cosmids were mapped by ...
Current mapping and sequencing strategies have been inadequate within the proximal portion of 19p12 ...
We have constructed and analysed somatic cell hybrids from cell lines containing balanced reciprocal...
Contains fulltext : mmubn000001_179492705.pdf (publisher's version ) (Open Access)...
A series of human-rodent somatic cell hybrids were investigated by Southern blot analysis for the pr...
Eight previously well-characterized and mapped probes derived from the human major histocompatibilit...
SIGLEAvailable from British Library Document Supply Centre-DSC:D064045 / BLDSC - British Library Doc...
SummaryMucolipidosis type IV (MLIV) is a lysosomal storage disorder characterized by severe neurolog...
The Philadelphia chromosome (Ph) resulting from translocation t(9;22)(q34;q11) is observed in more t...
Summary. Prenatal diagnosis in a fetus with holoprosence-phaly showed a 45,X karyotype and a suspect...
DNA sequence amplification contributes to the multistep process of carcinogenesis, and overexpressio...
We describe the application of fluorescence in situ hybridization (FISH) in a case of suspected chro...
Structural rearrangements involving the long arm of chromosome 19 characterize a cytogenetic subgrou...
In this study of ovarian carcinoma, we extended previous findings by performing FISH using chromosom...
The 1p/19q codeletion is the result of a translocation between chromosome 1 (Chr1p) and chromosome 1...
We report here the band location of 540 cosmids mapped to chromosome 19. The cosmids were mapped by ...
Current mapping and sequencing strategies have been inadequate within the proximal portion of 19p12 ...
We have constructed and analysed somatic cell hybrids from cell lines containing balanced reciprocal...
Contains fulltext : mmubn000001_179492705.pdf (publisher's version ) (Open Access)...
A series of human-rodent somatic cell hybrids were investigated by Southern blot analysis for the pr...
Eight previously well-characterized and mapped probes derived from the human major histocompatibilit...
SIGLEAvailable from British Library Document Supply Centre-DSC:D064045 / BLDSC - British Library Doc...
SummaryMucolipidosis type IV (MLIV) is a lysosomal storage disorder characterized by severe neurolog...
The Philadelphia chromosome (Ph) resulting from translocation t(9;22)(q34;q11) is observed in more t...
Summary. Prenatal diagnosis in a fetus with holoprosence-phaly showed a 45,X karyotype and a suspect...
DNA sequence amplification contributes to the multistep process of carcinogenesis, and overexpressio...
We describe the application of fluorescence in situ hybridization (FISH) in a case of suspected chro...
Structural rearrangements involving the long arm of chromosome 19 characterize a cytogenetic subgrou...
In this study of ovarian carcinoma, we extended previous findings by performing FISH using chromosom...
The 1p/19q codeletion is the result of a translocation between chromosome 1 (Chr1p) and chromosome 1...