Lethal presentation of mosaic tetrasomy 12p Pallister-Killian/syndromeYOUNG, I. D; DUCKETT, D. P; O'REILLY, K. M et al.Annales de génétique (Paris). 1989, Vol 32, Num 1, pp 62-64, issn 0003-3995, 3 p.Article

Deletion (12) (q 15 q 21.2)WATSON, M. S; MCALLISTER-BARTON, L; MAHONEY, M. J et al.Journal of medical genetics. 1989, Vol 26, Num 5, pp 343-344, issn 0022-2593, 2 p.Article

Intersitial del(12)(q15q22) in myelodysplastic syndromesFERRO, M. T; GARCIA-SAGREDO, J. M; RESINO, M et al.Cancer genetics and cytogenetics. 1995, Vol 80, Num 2, pp 158-159, issn 0165-4608Article

Chromosomal mosaicism in the Killian-Teschler-Nicola syndromeRAFFEL, L. J; MOHANDAS, T; RIMOIN, D. L et al.American journal of medical genetics. 1986, Vol 24, Num 4, pp 607-611, issn 0148-7299Article

Pallister-Killian syndrome : normal karyotype in prenatal chorionic villi, in postnatal lymphocytes, and in slowly growning epidermal cells, but mosaic tetrasomy 12p in skin fibroblastsHORN, D; MAJEWSKI, F; HILDEBRANDT, B et al.Journal of medical genetics. 1995, Vol 32, Num 1, pp 68-71, issn 0022-2593Article

Distal 12p delection in a Stillborn infantBARONCINI, A; AVELLINI, C; NERI, C et al.American journal of medical genetics. 1990, Vol 36, Num 3, pp 358-360, issn 0148-7299, 3 p.Article

Partial monosomy 12 p 13.1→13.3ROMAIN, D. R; GOLDSMITH, J; COLUMBANO-GREEN, L. M et al.Journal of medical genetics. 1987, Vol 24, Num 7, pp 434-436, issn 0022-2593Article

A new case of isolated del(12)(q15q22) in myelodysplastic syndromeFOWLER, Darren J; DEANGELO, Daniel J; ARIYANAYGAM, Shilani et al.Cancer genetics and cytogenetics. 2001, Vol 130, Num 1, pp 89-91, issn 0165-4608Article

Inv(12)(q15q24) : A nonrandom change associated with myelodysplasia?SCANTAMBURLO, G; LAMPERTZ, S; CROISIAU, C et al.Cancer genetics and cytogenetics. 2000, Vol 121, Num 2, pp 206-207, issn 0165-4608Article

Pallister-Killian syndrome : The first reported case in Hong KongLO, I. F.-M; CHEUNG, L. Y.-K; LAM, F. W.-F et al.Xiaoér keyi xuéhuì zázhì. 1998, Vol 39, Num 5, pp 333-335, issn 0001-6578Article

Identification of pericentric inversion 12, inv(12)(p13.lql i), by fluorescence in situ hybridization in a patient with acute myeloid leukemia (AML-M6)SATO, Y; BOHLANDER, S. K; KOBAYASHI, H et al.Cancer genetics and cytogenetics. 1997, Vol 97, Num 2, pp 157-160, issn 0165-4608Article

The ETV6, CDKN1B and D12S178 loci are involved in a segment commonly deleted in various 12p aberrations in different hematological malignanciesWLODARSKA, I; MARYNEN, P; LA STARZA, R et al.Cytogenetics and cell genetics. 1996, Vol 72, Num 2-3, pp 229-235, issn 0301-0171Conference Paper

Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocationSCOTT, J. A; WENGER, S. L; STEELE, M. W et al.American journal of medical genetics. 1995, Vol 56, Num 1, pp 67-71, issn 0148-7299Article

Pericentric inversion of chromosome 12 ; a three family studyHAAGERUP, A; HERTZ, J. M.Human genetics. 1992, Vol 89, Num 3, pp 292-294, issn 0340-6717Article

Prenatal diagnosis of pallister-killiam syndromeSOUKUP, S; NEIDICH, K.American journal of medical genetics. 1990, Vol 35, Num 4, pp 526-528, issn 0148-7299, 3 p.Article

A malignant mixed gonadal stromal tumor of the testis with heterologous components and i(12p) in one of its metastasesOOSTERHUIS, J. W; CASTEDO, S. M. M. J; DE JONG, B et al.Cancer genetics and cytogenetics. 1989, Vol 41, Num 1, pp 105-114, issn 0165-4608Article

A case of myxoid liposarcoma with translocation t(12;16) as the only abnormalityWALTER, T. A; DECKER, H.-J. H; LEONG, S. P. L et al.Cancer genetics and cytogenetics. 1988, Vol 34, Num 1, pp 117-118, issn 0165-4608Article

The origin of trisomy 12 in B-cell chronic lymphocytic leukemiaMECUCCI, C; DELANNOY, A; VAN DEN BERGHE, H et al.Cancer genetics and cytogenetics. 1988, Vol 36, Num 2, pp 203-204, issn 0165-4608Article

Ring chromosome 12PARK, J. P; GRAHAM, J. M. JR; ANDREWS, P. A et al.American journal of medical genetics. 1988, Vol 29, Num 2, pp 437-440, issn 0148-7299Article

Inversions of chromosome 12 in human malignanciesLARRIPA, I; MECUCCI, C; TESTONI, N et al.Cancer genetics and cytogenetics. 1987, Vol 28, Num 1, pp 113-118, issn 0165-4608Article

La tétrasomie 12p en mosaïque. Réunification du syndrome de Pallister, de Teschler-Nicola/Killian et de la tétrasomie 21 en mosaïque = Mosaïc tetrasomy 12p ― Pallister syndrome, Teschler-Nicola/Killian syndrome and tissular mosaïc tetrasomy 21. An analysis for reclassificationGILGENKRANTZ, S; FRYNS, J. P; DROULLE, P et al.Journal de génétique humaine. 1987, Vol 35, Num 1, pp 51-61, issn 0021-7743Article

Remaniement du petit bras du chromosome 12 dans les leucémies myélomonocytaires chroniques (LMMC) = Rearrangement of the short arm of chromosome 12 at band 12 in chronic myelomonocytic leukemia (CMMC)TANZER, J; LESSARD, M; GUILHOT, F et al.Nouvelle revue française d'hématologie. 1987, Vol 29, Num 1, pp 65-68, issn 0029-4810Article

Nonrandom involvement of the 12p12 breakpoint in chromosome abnormalities of childhood acute lymphoblastic leukemiaRAIMONDI, S. C; WILLIAMS, D. L; CALLIHAN, T et al.Blood. 1986, Vol 68, Num 1, pp 69-75, issn 0006-4971Article

Cytogenetic evidence for clonal evolution in B-cell chronic lymphocytic leukemiaTIN HAN; OHTAKI, K; SADAMORI, N et al.Cancer genetics and cytogenetics. 1986, Vol 23, Num 4, pp 321-328, issn 0165-4608Article

Involvement of chromosomes 12 and 14 in the cutaneous stage of mycosis fungoides: cytogenetic evidence for a multistep pathogenesis of the diseaseBARBIERI, D; SPANEDDA, R; CASTOLDI, G. L et al.Cancer genetics and cytogenetics. 1986, Vol 20, Num 3-4, pp 287-292, issn 0165-4608Article