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Haemophilia : the Official Journal of the World Federation of Hemophilia
|
October 1, 2015
X-linked moyamoya syndrome associated with severe haemophilia A
M Lavin, P V Jenkins, C Keenan, et al.
Pediatric Research
|
September 27, 2000
Inv(11)(p13p15) and myf-3(MyoD1) in a malignant extrarenal rhabdoid tumor of a premature newborn
F Staehelin, H Bissig, I Hösli, et al.
Genes, Chromosomes & Cancer
|
September 1, 1990
Monosomy 20: a nonrandom finding in childhood acute lymphoblastic leukemia
D R Betts, J E Kingston, E L Dorey, et al.
Genes, Chromosomes & Cancer
|
June 8, 2001
Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY)
N Cohen, D R Betts, L Trakhtenbrot, et al.
Blood
|
September 15, 1993
Isolated follicular lymphoma cells are resistant to apoptosis and can be grown in vitro in the CD40/stromal cell system
P W Johnson, S M Watt, D R Betts, et al.
Irish Journal of Medical Science
|
April 21, 2015
Unexplained developmental delay/learning disability: guidelines for best practice protocol for first line assessment and genetic/metabolic/radiological investigations
J J O'Byrne, S A Lynch, E P Treacy, et al.
Case Reports in Genetics
|
February 21, 2013
Duplication of 17q11.2 and Features of Albright Hereditary Osteodystrophy Secondary to Methylation Defects within the GNAS Cluster: Coincidence or Causal?
M White, J Conroy, H Bullman, et al.
British Journal of Haematology
|
June 10, 2000
Establishment and characterization of an arsenic-sensitive monoblastic leukaemia cell line (SigM5)
R Walter, G Schoedon, E Bächli, et al.
Leukemia
|
September 14, 2007
A simple FISH assay for the detection of 3q26 rearrangements in myeloid malignancy
V De Melo, M Vetter, H Mazzullo, et al.
British Journal of Cancer
|
June 28, 2002
Prognostic impact of chromosomal aberrations in Ewing tumours
C M Hattinger, U Pötschger, M Tarkkanen, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
October 1, 2015
X-linked moyamoya syndrome associated with severe haemophilia A
M Lavin, P V Jenkins, C Keenan, et al.
Pediatric Research
|
September 27, 2000
Inv(11)(p13p15) and myf-3(MyoD1) in a malignant extrarenal rhabdoid tumor of a premature newborn
F Staehelin, H Bissig, I Hösli, et al.
Genes, Chromosomes & Cancer
|
September 1, 1990
Monosomy 20: a nonrandom finding in childhood acute lymphoblastic leukemia
D R Betts, J E Kingston, E L Dorey, et al.
Genes, Chromosomes & Cancer
|
June 8, 2001
Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY)
N Cohen, D R Betts, L Trakhtenbrot, et al.
Blood
|
September 15, 1993
Isolated follicular lymphoma cells are resistant to apoptosis and can be grown in vitro in the CD40/stromal cell system
P W Johnson, S M Watt, D R Betts, et al.
Irish Journal of Medical Science
|
April 21, 2015
Unexplained developmental delay/learning disability: guidelines for best practice protocol for first line assessment and genetic/metabolic/radiological investigations
J J O'Byrne, S A Lynch, E P Treacy, et al.
Case Reports in Genetics
|
February 21, 2013
Duplication of 17q11.2 and Features of Albright Hereditary Osteodystrophy Secondary to Methylation Defects within the GNAS Cluster: Coincidence or Causal?
M White, J Conroy, H Bullman, et al.
British Journal of Haematology
|
June 10, 2000
Establishment and characterization of an arsenic-sensitive monoblastic leukaemia cell line (SigM5)
R Walter, G Schoedon, E Bächli, et al.
Leukemia
|
September 14, 2007
A simple FISH assay for the detection of 3q26 rearrangements in myeloid malignancy
V De Melo, M Vetter, H Mazzullo, et al.
British Journal of Cancer
|
June 28, 2002
Prognostic impact of chromosomal aberrations in Ewing tumours
C M Hattinger, U Pötschger, M Tarkkanen, et al.
Page
of 4