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Euchromatic variant 16p+. Implications in prenatal diagnosisLOPEZ PAJARES, I; VILLA, O; DELICADO, A et al.Prenatal diagnosis. 2006, Vol 26, Num 6, pp 535-538, issn 0197-3851, 4 p.Article

Inversion of chromosome 16 in accelerated phase of chronic myeloid leukaemia : report of a case and review of the literatureCOLOVIC, M; JANKOVIC, G; BILA, J et al.Medical oncology (Northwood). 1998, Vol 15, Num 3, pp 199-201, issn 1357-0560Article

Delineation of a ring chromosome 16 by the FISH-technique : a case report with reviewCONTE, R. A; KLEYMAN, S. M; KHARODE, C et al.Clinical genetics. 1997, Vol 51, Num 3, pp 196-199, issn 0009-9163Article

X/autosome translocation in three generations ascertained through an infant with trisomy 16p due to failure of spreading of X-inactivationPREIS, W; BARBI, G; LIPTAY, S et al.American journal of medical genetics. 1996, Vol 61, Num 2, pp 117-121, issn 0148-7299Article

De novo trisomy 16pCARRASCO JUAN, J. L; CIGUDOSA, J. C; OTERO GOMEZ, A et al.American journal of medical genetics. 1997, Vol 68, Num 2, pp 219-221, issn 0148-7299Article

A new cytogenetic subgroup in tenosynovial giant cell tumors (nodular tenosynovitis) is characterized by involvement of 16q24DAL CIN, P; SCIOT, R; DE SMET, L et al.Cancer genetics and cytogenetics. 1996, Vol 87, Num 1, pp 85-87, issn 0165-4608Article

Translocation (16;20)(p11.2;q13): sole cytogenetic abnormality in a unicameral bone cystRICHKIND, Kathleen E; MORTIMER, Errol; MOWERY-RUSHTON, Patricia et al.Cancer genetics and cytogenetics. 2002, Vol 137, Num 2, pp 153-155, issn 0165-4608Article

Translocation (16;17)(q22;p13) is a recurrent anomaly of aneurysmal bone cystsHERENS, Christian; THIRY, Albert; DRESSE, Marie Francoise et al.Cancer genetics and cytogenetics. 2001, Vol 127, Num 1, pp 83-84, issn 0165-4608Article

Identification of the inverted chromosome 16 using chromosome paintingNAGESHRAO, P; FLEJTER, W. L; RAHI, S et al.British journal of haematology. 1999, Vol 104, Num 3, pp 618-620, issn 0007-1048Article

Consistent detection of TLS/FUS-ERG chimeric transcripts in acute myeloid leukemia with t(16;21)(p11;q22) and identification of a novel transcriptKONG, X.-T; IDA, K; MIURA, I et al.Blood. 1997, Vol 90, Num 3, pp 1192-1199, issn 0006-4971Article

Familial reciprocal translocation t(7;16) associated with maternal uniparental disomy 7 in a Silver-Russell patientDUPONT, Jean-Michel; CUISSET, Laurence; CARTIGNY, Maryse et al.American journal of medical genetics. 2002, Vol 111, Num 4, pp 405-408, issn 0148-7299Article

Two more Inv(16) acute myeloid leukemia cases with infrequent CBFβ-MYH11 fusion transcript: clinical and molecular findingsMARTINELLI, Giovanni; OTTAVIANI, Emanuela; BUONAMICI, Silvia et al.Haematologica (Roma). 2002, Vol 87, Num 5, pp 554-555, issn 0390-6078Article

Comparative genomic hybridization defines frequent loss on 16p in human anaplastic thyroid carcinomaKOMOIKE, Y; TAMAKI, Y; OHNISHI, T et al.International journal of oncology. 1999, Vol 14, Num 6, pp 1157-1162, issn 1019-6439Article

Chromosome 16 inversion-associated translocation : Two new casesMAAREK, O; SALABELLE, A; BUSSON LE CONIAT, M et al.Cancer genetics and cytogenetics. 1999, Vol 114, Num 2, pp 126-129, issn 0165-4608Article

Karyotypic evolution in breast carcinomas with i(1)(q10) and der(1;16)(q10;p10) as the primary chromosome abnormalityTSAROUHA, H; PANDIS, N; BARDI, G et al.Cancer genetics and cytogenetics. 1999, Vol 113, Num 2, pp 156-161, issn 0165-4608Article

Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3CLETON-JANSEN, A.-M; MOERLAND, E. W; CORNELISSE, C. J et al.British journal of cancer. 1999, Vol 79, Num 7-8, pp 1049-1052, issn 0007-0920Article

Complex chromosome rearrangement involving chromosomes 1, 4 and 16 revealed by fluorescence in situ hybridizationJOHANNESSON, T; EHLERS, S; WAHLSTRÖM, J et al.Clinical genetics. 1997, Vol 51, Num 4, pp 281-285, issn 0009-9163Article

Pericentric inversion of chromosome 16 and eosinophilia in chronic myelomonocytic leukemiaMIYAMOTO, T; AKASHI, K; HAYASHI, S et al.Cancer genetics and cytogenetics. 1997, Vol 94, Num 2, pp 99-102, issn 0165-4608Article

Acute myelogenous leukemia : a disorder of gene splicing ?VAN DER REIJDEN, B. A; VAN OMMEN, G-J; HAGEMEIJER, A et al.Leukemia. 1996, Vol 10, Num 2, pp 204-206, issn 0887-6924Article

Allelic loss of chromosome 16q in endometrial cancer : Correlation with poor prognosis of patients and less differentiated histologyKIHANA, T; YANO, N; MURAO, S.-I et al.Japanese journal of cancer research. 1996, Vol 87, Num 11, pp 1184-1190, issn 0910-5050Article

Constitutional t(16;22)(pl3.3;q11.2∼12) in a primitive neuroectodermal tumor of the pineal regionSAWYER, Jeffrey R; SAMMARTINO, Gael; HUSAIN, Muhammad et al.Cancer genetics and cytogenetics. 2003, Vol 142, Num 1, pp 73-76, issn 0165-4608, 4 p.Article

Loss of heterozygosity on chromosome 16p and 18q in anaplastic thyroid carcinomaKADOTA, Masao; TAMAKI, Yasuhiro; SEKIMOTO, Mitsugu et al.Oncology reports. 2003, Vol 10, Num 1, pp 35-38, issn 1021-335X, 4 p.Article

Molecular rulers for calibrating phenotypic effects of telomere imbalanceMARTIN, C. L; WAGGONER, D. J; LEDBETTER, D. H et al.Journal of medical genetics. 2002, Vol 39, Num 10, pp 734-740, issn 0022-2593Article

Deletion of 16q11 is a recurrent cytogenetic aberration in acute myeloblastic leukemia during disease progressionYAMAMOTO, Katsuya; NAGATA, Kaoru; KIDA, Aiko et al.Cancer genetics and cytogenetics. 2001, Vol 131, Num 1, pp 65-68, issn 0165-4608Article