Unusual phenotype in partial trisomy 14LEMIRE, E. G; CARDWELL, S.American journal of medical genetics. 1999, Vol 87, Num 4, pp 294-296, issn 0148-7299Article

Unbalanced karyotype, dup 14(q13-q22), in a mother and her two childrenPOT, M. L. H; GILTAY, J. C; VAN WILSEN, A et al.Clinical genetics. 1996, Vol 50, Num 5, pp 398-402, issn 0009-9163Article

Deletions at 14q in malignant mesothelioma detected by microsatellite marker analysisBJÖRKQVIST, A.-M; WOLF, M; NORDLING, S et al.British journal of cancer. 1999, Vol 81, Num 7, pp 1111-1115, issn 0007-0920Article

Need for search for cryptic translocation in parents with several children affected with mca : Report of a cryptic translocation (10;14) detected by FISHDELNESTE, D; VAMOS, E; PIERQUIN, G et al.Genetic counseling. 1998, Vol 9, Num 2, pp 97-102, issn 1015-8146Conference Paper

Delineation of 14q32.3 deletion syndromeORTIGAS, A. P; STEIN, C. K; THOMSON, L. L et al.Journal of medical genetics. 1997, Vol 34, Num 6, pp 515-517, issn 0022-2593Article

The Translocation t(4;14) Can Be Present Only in Minor Subclones in Multiple MyelomaHEBRAUD, Benjamin; CAILLOT, Denis; VOILLAT, Laurent et al.Clinical cancer research (Print). 2013, Vol 19, Num 17, pp 4634-4637, issn 1078-0432, 4 p.Article

Defining the breakpoints of proximal chromosome 14q rearrangements in nine patients using flow-sorted chromosomesKAMNASARAN, Deepak; O'BRIEN, Patricia C. M; SCHUFFENHAUER, Simone et al.American journal of medical genetics. 2001, Vol 102, Num 2, pp 173-182, issn 0148-7299Article

Chromosomal anomalies in a case of proliferative myositisMCCOMB, E. N; NEFF, J. R; JOHANSSON, S. L et al.Cancer genetics and cytogenetics. 1997, Vol 98, Num 2, pp 142-144, issn 0165-4608Conference Paper

Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formationPAGE, S. L; SHIN, J.-C; HAN, J.-Y et al.Human molecular genetics (Print). 1996, Vol 5, Num 9, pp 1279-1288, issn 0964-6906Article

Maternal uniparental disomy of chromosome 14 confined to an interstitial segment (14q23-14q24.2)MARTIN, R. A; SABOL, D. W; ROGAN, P. K et al.Journal of medical genetics. 1999, Vol 36, Num 8, pp 633-636, issn 0022-2593Article

Trisomy 14 and leukemiaREDDY, K. S.Cancer genetics and cytogenetics. 1998, Vol 106, Num 2, pp 144-151, issn 0165-4608Article

Twin pregnancy discordant for trisomy 14 mosaicism : Prenatal sonographic findingsSEPULVEDA, W; MONCKEBERG, M. J; BE, C et al.Prenatal diagnosis. 1998, Vol 18, Num 5, pp 481-484, issn 0197-3851Article

Is t(6;14) a non-random translocation in childhood acute mixed lineage leukemia ?BATANIAN, J. R; DUNPHY, C. H; GALE, G et al.Cancer genetics and cytogenetics. 1996, Vol 90, Num 1, pp 29-32, issn 0165-4608Article

Isochromosome 14q in refractory anemiaBOAVIDA, M. G; AMBROSIO, P; DHERMY, D et al.Cancer genetics and cytogenetics. 1997, Vol 97, Num 2, pp 155-156, issn 0165-4608Article

Another patient with a deletion 14qll.2q13GOVAERTS, L; TOORMAN, J; BLIJ-PHILIPSEN, M. V. D et al.Annales de génétique (Paris). 1996, Vol 39, Num 4, pp 197-200, issn 0003-3995Article

Agammaglobulinämie bei einem gemischtgeschlechtlichen geschwisterpaar mit dem phänotypischen Bild des Morbus Bruton = Agammaglobulinemia in a brother and sister with the clinical aspect of Bruton's diseaseTRÜBEL, H; HABERMEHL, P; SCHNEIDER, T et al.Monatsschrift für Kinderheilkunde. 1998, Vol 146, Num 8, pp 754-757, issn 0026-9298Article

Sperm nuclei analysis of a Robertsonian t(14q21q) carrier, by FISH, using three plasmids and two YAC probesROUSSEAUX, S; CHEVRET, E; MONTEIL, M et al.Human genetics. 1995, Vol 96, Num 6, pp 655-660, issn 0340-6717Article

Age-Dependent Prevalence and Frequency of Circulating t(14;18)-Positive Cells in the Peripheral Blood of Healthy IndividualsDOLKEN, Gottfried; DOLKEN, Lars; HIRT, Carsten et al.Journal of the National Cancer Institute. Monographs. 2008, Vol 39, pp 44-47, issn 1052-6773, 4 p.Conference Paper

Hypomelanosis of Ito and a 'mirror image' whole chromosome duplication resulting in trisomy 14 mosaicismTUNCA, Y; WILROY, R. S; KADANDALE, J. S et al.Annales de génétique (Paris). 2000, Vol 43, Num 1, pp 39-43, issn 0003-3995Article

Loss of heterozygosity at D14S62 and metastatic potential of breast cancerO'CONNELL, P; FISCHBACH, K; HILSENBECK, S et al.Journal of the National Cancer Institute. 1999, Vol 91, Num 16, pp 1391-1397, issn 0027-8874Article

Translocation (3;14)(q27;q11) : A new variant translocation in a patient with non-Hodgkin's lymphoma of B-cell type with BCL6 rearrangementTAKAHASHI, N; MIURA, I; HIROSAWA, S et al.Cancer genetics and cytogenetics. 1996, Vol 90, Num 1, pp 49-53, issn 0165-4608Article

Hyperdiploidy is less frequent in AL amyloidosis compared with monoclonal gammopathy of undetermined significance and inversely associated with translocation t( 11;14)BOCHTLER, Tilmann; HEGENBART, Ute; HO, Anthony D et al.Blood. 2011, Vol 117, Num 14, pp 3809-3815, issn 0006-4971, 7 p.Article

Detailed deletion mapping of chromosome band 14q32 in human neuroblastoma defines a 1.1-Mb region of common allelic lossHOSHI, M; OTAGIRI, N; SHIWAKU, H et al.British journal of cancer. 2000, Vol 82, Num 11, pp 1801-1807, issn 0007-0920Article

Pure partial trisomy 5q33→5q35 resulting from the adjacent-1 segregation of a paternal (5;14)(q33;p12) translocationPAOLONI-GIACOBINO, A; BOTTANI, A; DAHOUN, S. P et al.Annales de génétique (Paris). 1999, Vol 42, Num 3, pp 166-169, issn 0003-3995Conference Paper

Low number of DNA copy number changes in small lymphocytic lymphomaAUTIO, K; AALTO, Y; FRANSSILA, K et al.Haematologica - Journal of hematology. 1998, Vol 83, Num 8, pp 690-692Article