|1.||Hadjistilianou, Theodora: 2 articles (09/2012 - 04/2002)|
|2.||De Francesco, Sonia: 2 articles (09/2012 - 04/2002)|
|3.||Mastrangelo, Domenico: 2 articles (09/2012 - 04/2002)|
|4.||Aguilera, Zenia P: 1 article (10/2015)|
|5.||Jayakar, Parul: 1 article (10/2015)|
|6.||Cavuoto, Kara M: 1 article (10/2015)|
|7.||Belin, Peter J: 1 article (10/2015)|
|8.||McKeown, Craig A: 1 article (10/2015)|
|9.||Hirakata, Kyoko: 1 article (08/2015)|
|10.||Shiihara, Takashi: 1 article (08/2015)|
07/28/2009 - "[Chromosome 13q deletion detected by interphase FISH in multiple myeloma: a study of 100 cases in China]."
10/08/2007 - "Chromosome 13q deletion and IgH abnormalities may be both masked by near-tetraploidy in a high proportion of multiple myeloma patients: a combined morphology and I-FISH analysis."
|2.||Retinoblastoma (Glioblastoma, Retinal)
09/01/2012 - "Dysmorphic features in children must be always suspicious of 13q deletion syndrome and a short ophthalmoscopic follow-up is necessary to detect the presence of a retinoblastoma."
09/01/2012 - "To report the case of identical dichorionic diamniotic female twins with unilateral retinoblastoma in 13q deletion syndrome. "
09/01/2012 - "13q deletion syndrome and retinoblastoma in identical dichorionic diamniotic monozygotic twins."
03/01/2010 - "Axenfeld-Rieger ocular anomaly and retinoblastoma caused by constitutional chromosome 13q deletion."
03/01/2007 - "Chromosomal analysis revealed partial chromosome 13q deletion involving band 14 which is associated with a high risk of retinoblastoma. "
03/15/2013 - "Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: phenotypic and genotypic findings."
10/01/2012 - "Whereas patients with unfavorable (deletion 17p, deletion 11q) and intermediate (trisomy 12, normal FISH) cytogenetics with concomitant t(IGH@) had similar median treatment-free survival (TFS) as those without a t(IGH@), patients with deletion 13q (del13q) and a t(IGH@) had significantly worse TFS than those without a t(IGH@): median TFS 4.7 versus 8.0 years, P = 0.03 (hazard ratio 4.21, 95% confidence interval 1.06-16.69 y, P = 0.04 in multivariate analysis after adjusting for age, sex, Rai stage, and white blood cell count). "
11/01/2010 - "Cases were categorized hierarchically into deletion(17p), deletion(11q), trisomy 12, deletion(13q) as sole abnormality or normal karyotype. "
03/01/2007 - "Ras mutations did not correlate with the presence of chromosome 13q deletion, trisomy of chromosome 11, 1q amplification or hyperdiploidy. "
08/01/2003 - "We investigated genome changes in 12 hypermutated cases (M-CLL) and 22 unmutated cases (UM-CLL) by use of comparative genomic hybridization, G-banding, and multicolor fluorescence in situ hybridization (m-FISH) after optimal mitogen stimulation and FISH analysis of typical CLL aberrations: 11q deletion, 13q deletion, and trisomy 12. "
|4.||Chromosome Aberrations (Chromosome Abnormalities)
01/01/2014 - "The clinical features of 13q deletion syndrome, a rare chromosomal abnormality, were originally described in the early 1960s, though the literature currently lacks defined phenotypic abnormalities. "
11/15/2008 - "Molecular cytogenetic abnormalities identified by fluorescent in situ hybridization in A-GBM, E-GBM, and TE-GBM, respectively, included p16 deletion/-9 (60%, 71%, 64%); chromosome 10 loss (40%, 63%, 57%), chromosome 7 gain without EGFR amplification (70%, 38%, 40%), EGFR amplification (10%, 50%, 27%), PTEN deletion (10%, 25%, 29%), PDGFRA amplification (10%, 25%, 0%), and RB1 deletion/-13q (50%, 0%, 14%). "
06/01/1997 - "Chromosome 13q deletion is among the most common cytogenetic abnormalities in chronic lymphocytic leukaemia (CLL). "
02/01/2002 - "The regularity of surface membrane antigen expression patterns, their interrelationships as well as the effects of the three frequent chromosomal aberrations, ie 11q deletion, 13q deletion and trisomy 12, were investigated in 35 classic CLL cases by flow cytometry. "
08/01/2015 - "Holoprosencephaly with cerebellar vermis hypoplasia in 13q deletion syndrome: Critical region for cerebellar dysgenesis within 13q32.2q34."
03/01/2002 - "Unusual variant of holoprosencephaly in monosomy 13q."
01/01/2015 - "We present a new case with 13q deletion syndrome phenotypically characterized by severe major malformations, some of them still undescribed, consisting of left diaphragmatic hernia, right pulmonary sequestration, hypoplastic left heart syndrome, pancreatic agenesis, polysplenia, and catastrophic central nervous system malformations: semilobar holoprosencephaly, occipital myelomeningocele, partial agenesis of the corpus callosum and agenesis of olfactory bulbs. "
|2.||Immunoglobulin Light Chains (Immunoglobulin Light Chain)
|3.||Immunoglobulin Heavy Chains (Immunoglobulin Heavy Chain)
|6.||monosomy 6q Chromosome 6
|7.||Dandy Walker variant
|2.||Bone Marrow Transplantation (Transplantation, Bone Marrow)