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Chromosome 10 qter deletion syndromeCOSTAKOS, D. T; LOVE, L. A; JOSEPHSON, K et al.Archives of pediatrics & adolescent medicine. 1998, Vol 152, Num 5, pp 507-508, issn 1072-4710Article

Partial trisomy 10q : Further delineation of the clinical manifestations involving the segment 10q23→10q24HALPERN, G. J; SHOHAT, M; MERLOB, P et al.Annales de génétique (Paris). 1996, Vol 39, Num 3, pp 181-183, issn 0003-3995Article

dup(10q) Lacking α-satellite DNA in bone marrow cells of a patient with acute myeloid leukemiaABELIOVICH, D; YEHUDA, O; BEN-NERIAH, S et al.Cancer genetics and cytogenetics. 1996, Vol 89, Num 1, pp 1-6, issn 0165-4608Article

Pure trisomy lop resulting from an extra ring chromosome: Characterization by methods of advanced molecular cytogeneticsZHONG CHEN; MELONI-EHRIG, Aurelia; PALUMBOS, Janice C et al.American journal of medical genetics. 2001, Vol 102, Num 4, pp 379-382, issn 0148-7299Article

Duplication 10q22.1-q25.1 due to intrachromosomal insertion : A second caseGOSS, P. W; VOULLAIRE, L; GARDNER, R. J. M et al.Annales de génétique (Paris). 1998, Vol 41, Num 3, pp 161-163, issn 0003-3995Conference Paper

Unbalanced translocation in a mother and her son in one of two 5;10 translocation familiesBARBER, J. C. K; TAMPLE, I. K; CAMPBELL, P. L et al.American journal of medical genetics. 1996, Vol 62, Num 1, pp 84-90, issn 0148-7299Article

Maternal uniparental isodisomy 10 and mosaicism for an additional marker chromosome derived from the paternal chromosome 10 in a fetusSCHLEGEL, Monika; BAUMER, Alessandra; RIEGEL, Mariluce et al.Prenatal diagnosis. 2002, Vol 22, Num 5, pp 418-421, issn 0197-3851Article

Inv(10)(p11.2q21.2), a variant chromosomeCOLLINSON, M. N; FISHER, A. M; WALKER, J et al.Human genetics. 1997, Vol 101, Num 2, pp 175-180, issn 0340-6717Article

Partial trisomy of chromosome 10 inherited from a carrier fatherSESHADRI SURESH; INDRANI SURESH; PREMA LAKSHMINARAYANA et al.Indian journal of pediatrics. 1995, Vol 62, Num 5, pp 615-618, issn 0019-5456Article

Pure trisomy 10p involving an isochromosome 10pBEREND, S. A; SHAFFER, L. G; BEJJANI, B. A et al.Clinical genetics. 1999, Vol 55, Num 5, pp 367-371, issn 0009-9163Article

10q Deletions in metastatic cutaneous melanomaINDSTO, J. O; HOLLAND, E. A; KEFFORD, R. F et al.Cancer genetics and cytogenetics. 1998, Vol 100, Num 1, pp 68-71, issn 0165-4608Article

Terminal deletion of the long arm of chromosome 10 : A new case with breakpoint in q25.3PETERSEN, B; STRASSBURG, H.-M; FEICHTINGER, W et al.American journal of medical genetics. 1998, Vol 77, Num 1, pp 60-62, issn 0148-7299Article

Terminal deletion of chromosome 10q26 : Delineation of two clinical phenotypesPETIT, P; DEVRIENDT, K; AZOU, M et al.Genetic counseling. 1998, Vol 9, Num 4, pp 271-275, issn 1015-8146Conference Paper

A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11→q223 ?VAN BUGGENHOUT, G; DECOCK, P; FRYNS, J. P et al.Genetic counseling. 1996, Vol 7, Num 1, pp 53-59, issn 1015-8146Conference Paper

Mutational analysis of the PTEN/MMAC1 gene in non-Hodgkin's lymphomaNAKAHARA, Y; NAGAI, H; KINOSHITA, T et al.Leukemia. 1998, Vol 12, Num 8, pp 1277-1280, issn 0887-6924Article

Familial four breakpoint complex chromosomal rearrangement as a cause of monosomy 9p22→pter and trisomy 10p11.2→pter and 11q21 analysed by dual and triple colour fishSTANKIEWICZ, P; KOSTYK, E; BOCIAN, E et al.Journal of medical genetics. 1997, Vol 34, Num 8, pp 696-699, issn 0022-2593Article

A 3 1/2 old girl with distal trisomy 19q defined by FISHJAMES, C; JAUCH, A; ROBSON, L et al.Journal of medical genetics. 1996, Vol 33, Num 9, pp 795-797, issn 0022-2593Article

Acute leukemia with t(10;11)(p11-p15;q13-q23)SECCO, C; WIERNIK, P. H; BENNETT, J. M et al.Cancer genetics and cytogenetics. 1996, Vol 86, Num 1, pp 31-34, issn 0165-4608Article

Allelic loss on chromosome 10 in prostate adenocarcinomaITTMANN, M.Cancer research (Baltimore). 1996, Vol 56, Num 9, pp 2143-2147, issn 0008-5472Article

Translocation (X;10)(p10;p10) : A rare but nonrandom chromosomal abnormality in acute leukemia of myeloid differentiationWONG, K. F; HAYES, K. J; HUH, Y. O et al.Cancer genetics and cytogenetics. 1996, Vol 86, Num 2, pp 153-155, issn 0165-4608Article

Involvement of MLL gene in a t(10;11)(q22;q23) and a t(8;11)(q24;q23) identified by fluorescence in situ hybridizationAVENTIN, A; LA STARZA, R; MARTINEZ, C et al.Cancer genetics and cytogenetics. 1999, Vol 108, Num 1, pp 48-52, issn 0165-4608Article

Bilateral cryptorchidism associated with terminal deletion of 10qSUZUKI, Y; SASAGAWA, I; NAKADA, T et al.Urologia Internationalis. 1998, Vol 61, Num 3, pp 186-187, issn 0042-1138Article

De novo der(X)t(X;10)(q26;q21) with features of distal trisomy 10q : case report of paternal origin identified by late replication with BrdU and the human androgen receptor assay (HAR)GARCIA-HERAS, J; MARTIN, J. A; WITCHEL, S. F et al.Journal of medical genetics. 1997, Vol 34, Num 3, pp 242-245, issn 0022-2593Article

Disruption of the MMAC1/PTEN gene by deletion or mutation is a frequent event in malignant melanomaGULDBERG, P; THOR STRATEN, P; BIRCK, A et al.Cancer research (Baltimore). 1997, Vol 57, Num 17, pp 3660-3663, issn 0008-5472Article