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A supernumerary marker chromosome originating from two different regions of chromosome 18RÖTHLISBERGER, B; CHRZANOWSKA, K; BALMER, D et al.Journal of medical genetics. 2000, Vol 37, Num 2, pp 121-124, issn 0022-2593Article

Identification of supernumerary marker chromosomes derived from chromosomes 5, 6, 19, and 20 using FISHSTANKIEWICZ, P; BOCIAN, E; JAKUBOW-DURSKA, K et al.Journal of medical genetics. 2000, Vol 37, Num 2, pp 114-120, issn 0022-2593Article

Renal tubular dysgenesis, absent nipples, and multiple malformations in three brothers : A new, lethal syndromeHISAMA, F. M; REYES-MUGICA, M; WARGOWSKI, D. S et al.American journal of medical genetics. 1998, Vol 80, Num 4, pp 335-342, issn 0148-7299Article

Detection of sex-determining region in a male with chromosomal abnormality (46,X+MAR) and hypospadiasHAYASHI, Y; TSUGAYA, M; SASAKI, S et al.Urologia Internationalis. 1996, Vol 56, Num 2, pp 122-124, issn 0042-1138Article

Characterization of a small supernumerary ring X chromosoma by fluorescence in situ hydridizationDUNCAN, A. M. V; MACDONALD, A; BROWN, C. J et al.American journal of medical genetics. 1993, Vol 47, Num 8, pp 1153-1156, issn 0148-7299Article

Supernumerary marker chromosomes derived from chromosome 15: Analysis of 32 new casesEGGERMANN, K; MAU, U. A; BUJDOSO, G et al.Clinical genetics. 2002, Vol 62, Num 1, pp 89-93, issn 0009-9163Article

Clinical applications of primed in situ labelling (PRINS) rapid identification of a marker chromosome in a fetusVELAGALETI, G. V. N; CARPENTER, N. J; THARAPEL, A. T et al.Annales de génétique (Paris). 1997, Vol 40, Num 3, pp 154-157, issn 0003-3995Article

Efficient identification of marker chromosomes in 27 patients by stepwise hybridization with alpha-satellite DNA probesPLATTNER, R; HEEREMA, N. A; YUROV, Y. B et al.Human genetics. 1993, Vol 91, Num 2, pp 131-140, issn 0340-6717Article

Characterization of an analphoid, neocentromere-positive inv dup 8p marker chromosome using multiplex whole chromosome and sub-telomere FISH analysesVELINOV, M; GU, H; GENOVESE, M et al.Annales de génétique (Paris). 2004, Vol 47, Num 2, pp 199-205, issn 0003-3995, 7 p.Article

Delineation of supernumerary marker chromosomes in 38 patientsVIERSBACH, R; ENGELS, H; GAMERDINGER, U et al.American journal of medical genetics. 1998, Vol 76, Num 4, pp 351-358, issn 0148-7299Article

A large analphoid invdup(3)(q22.3qter) marker chromosome characterized by array-CGH in a child with malformations, mental retardation, ambiguous genitalia and Blaschko's linesGIMELLI, G; GIORDA, R; BERI, S et al.European journal of medical genetics. 2007, Vol 50, Num 4, pp 264-273, issn 1769-7212, 10 p.Article

Double supernumerary isodicentric chromosomes derived from 15 resulting in partial hexasomyQUMSIYEH, Mazin B; RAFI, Syed K; SARRI, Catherine et al.American journal of medical genetics. 2003, Vol 116A, Num 4, pp 356-359, issn 0148-7299, 4 p.Article

Coamplification of 12p11 and 12q13∼q22 in multiple ring chromosomes in a spindle cell sarcoma resolved by novel multicolor fluorescence in situ hybridization analysisLESTOU, Valia S; O'CONNELL, John X; LUDKOVSKI, Olga et al.Cancer genetics and cytogenetics. 2002, Vol 139, Num 1, pp 44-47, issn 0165-4608, 4 p.Article

Triplication of 1q in Fanconi anemiaFERRO, M. Teresa; VAZQUEZ-MAZARIEGO, Yolanda; RAMIRO, Soraya et al.Cancer genetics and cytogenetics. 2001, Vol 127, Num 1, pp 38-41, issn 0165-4608Article

Skin pigmentary anomalies and mosaicism for an acentric marker chromosome originating from 3qPORTNOÏ, M.-F; BOUTCHNEÏ, S; BOUSCARAT, F et al.Journal of medical genetics. 1999, Vol 36, Num 3, pp 246-250, issn 0022-2593Article

Confirming the origin of add(9q) and marker chromosome in a case of acute monoblastic leukemia (M5b) by fluorescence in situ hybridizationWONG, N; BOLI FAN; YEO, W et al.Cancer genetics and cytogenetics. 1998, Vol 106, Num 1, pp 87-89, issn 0165-4608Article

Characterization of a supernumerary small marker X chromosome in two females with similar phenotypesTÜMER, Z; WOLFF, D; SILAHTAROGLU, A. N et al.American journal of medical genetics. 1998, Vol 76, Num 1, pp 45-50, issn 0148-7299Article

Supernumerary marker 15 chromosomes : a clinical, molecular and FISH approach to diagnosis and prognosisCROLLA, J. A; HARVEY, J. F; SITCH, F. L et al.Human genetics. 1995, Vol 95, Num 2, pp 161-170, issn 0340-6717Article

Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridizationPLATTNER, R; HEEREMA, N. A; HOWARD-PEEBLES, P. N et al.Human genetics. 1993, Vol 91, Num 6, pp 589-598, issn 0340-6717Article

Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new casesCHANTOT-BASTARAUD, Sandra; MUTI, Christine; PIPIRAS, Eva et al.Annales de génétique (Paris). 2004, Vol 47, Num 3, pp 241-249, issn 0003-3995, 9 p.Article

A series of supernumerary small ring marker autosomes identified by FISH with chromosome probe arrays and literature review excluding chromosome 15DANIEL, Art; MALAFIEJ, Paul.American journal of medical genetics. 2003, Vol 117A, Num 3, pp 212-222, issn 0148-7299, 11 p.Article

Genomic rearrangements involving rDNA and centromeric heterochromatin in vulvar epidermoid carcinoma cell line A-431PEDRAZZINI, Estela; MAMAEV, Nikolai; YAKOVLEVA, Tatyana et al.Cancer genetics and cytogenetics. 2003, Vol 143, Num 1, pp 50-58, issn 0165-4608, 9 p.Article

True hermaphroditism with 46,X, +22p/46,XY and gonadal mosaicism detected by fluorescence in situ hybridizationTAKANO, Takako; YAMANOUCHI, Yasuko; TANAKA, Fumihiko et al.Annales de génétique (Paris). 2003, Vol 46, Num 1, pp 57-60, issn 0003-3995, 4 p.Article

Tetrasomy 15q25.3 → qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral wilms tumorsHU, J; MCPHERSON, E; SURTI, U et al.American journal of medical genetics. 2002, Vol 113, Num 1, pp 82-88, issn 0148-7299, 7 p.Article