Mechanisms and Consequences of Small Supernumerary Marker Chromosomes : From Barbara McClintock to Modern Genetic-Counseling IssuesBALDWIN, Erin L; MAY, Lorraine F; JUSTICE, April N et al.American journal of human genetics. 2008, Vol 82, Num 2, pp 398-410, issn 0002-9297, 13 p.Article

Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexityROBERTS, S. E; MAGGOUTA, F; THOMAS, N. S et al.American journal of human genetics. 2003, Vol 73, Num 5, pp 1061-1072, issn 0002-9297, 12 p.Article

Primed IN Situ labelling (PRINS) as a rational procedure for identification of marker chromosomes using a panel of primers differentially tagging the human chromosomesHINDKJAER, J; BRANDT, C. A; STRØMKJAER, H et al.Clinical genetics. 1996, Vol 50, Num 6, pp 437-441, issn 0009-9163Article

Supernumerary Marker Chromosomes Management in Prenatal DiagnosisGRUCHY, Nicolas; LEBRUN, Marine; HERLICOVIEZ, Michel et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 21, pp 2770-2776, issn 1552-4825, 7 p.Article

Monte carlo pedigree disequilibrium test for markers on the X chromosomeJIE DING; SHILI LIN; YANG LIU et al.American journal of human genetics. 2006, Vol 79, Num 3, pp 567-573, issn 0002-9297, 7 p.Article

Molecular charaterization of two extra marker chromosomes detected at prenatal diagnosisCALABRESE, G; STUPPIA, L; MINGARELLI, R et al.Annales de génétique (Paris). 1994, Vol 37, Num 3, pp 135-138, issn 0003-3995Article

RETINOBLASTOMA. A MODEL OF HEREDITARY FRAGILE CHROMOSOMAL REGIONS = LE RETINOBLASTOME. UN MODELE DE REGIONS CHROMOSOMIQUES FRAGILES HEREDITAIRESNEMAT HASHEM; KHALIFA S.1975; HUM. HERED.; SWITZ.; DA. 1975; VOL. 25; NO 1; PP. 35-49; BIBL. 14REF.Article

CHROMOSOME CONSTITUTION OF TRANSITIONAL CELL CARCINOMA OF THE URINARY BLADDER = CONSTITUTION CHROMOSOMIQUE DU CANCER A CELLULES DE TRANSITION DE LA VESSIE1972; CANCER; U.S.A.; DA. 1972; VOL. 29; NO 5; PP. 1401-1412; BIBL. 19 REF.Serial Issue

Tetrasomy 13q31.1qter Due To an Inverted Duplicated Neocentric Marker Chromosome in a Fetus With Multiple MalformationsHADDAD, Véronique; ABOURA, Azzedine; TOSCA, Lucie et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 4, pp 894-900, issn 1552-4825, 7 p.Article

Characterization of an analphoid supernumerary marker chromosome derived from 15q25→qter using high-resolution CGH and multiplex FISH analysesHUANG, X.-L; DE MICHELENA, M. I; MARK, H. F. L et al.Clinical genetics. 2005, Vol 68, Num 6, pp 513-519, issn 0009-9163, 7 p.Article

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

Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridizationDARNAUDE, M. T; DIAZ DE BUSTAMANTE, A; CABELLO, P et al.Annales de génétique (Paris). 1996, Vol 39, Num 2, pp 61-63, issn 0003-3995Article

Marker chromosome identification by micro-FISHENGELEN, J. J. M; LOOTS, W. J. G; MOTOH, P. C. C et al.Clinical genetics. 1996, Vol 49, Num 5, pp 242-248, issn 0009-9163Article

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

Identification of marker chromosomes in thirteen patients using FISH probingDANIEL, A; MALAFIEJ, P; PREECE, K et al.American journal of medical genetics. 1994, Vol 53, Num 1, pp 8-18, issn 0148-7299Article

Chromosome 14 marker appearance in a human B lymphoblastoid cell line of nonmalignant originYANDELL, D. W; LITTLE, J. B.Cancer genetics and cytogenetics. 1986, Vol 20, Num 3-4, pp 231-239, issn 0165-4608Article

Neocentromere Marker Chromosome of Distal 3q Mimicking dup(3q) Syndrome PhenotypeIZUMI, Kosuke; YAMASHITA, Yukio; ARAMAKI, Michihiko et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 15, pp 1967-1971, issn 1552-4825, 5 p.Article

Characterization of six marker chromosomes by comparative genomic hybridizationBELLOSO, J. M; CABALLIN, M. R; GABAU, E et al.American journal of medical genetics. 2005, Vol 136A, Num 2, pp 169-174, issn 0148-7299, 6 p.Article

Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosisGUANCIALI-FRANCHI, Paolo; CALABRESE, Giuseppe; ZATTERALE, Adriana et al.American journal of medical genetics. 2004, Vol 127A, Num 2, pp 144-148, issn 0148-7299, 5 p.Article

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

Small marker X chromosomes lack the X inactivation center : implications for karyotype/phenotype correlationsWOLFF, D. J; BROWN, C. J; SCHWARTZ, S et al.American journal of human genetics. 1994, Vol 55, Num 1, pp 87-95, issn 0002-9297Article

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

Mosaic 5p tetrasomySTANLEY, W. S; POWELL, C. M; DEVINE, G. C et al.American journal of medical genetics. 1993, Vol 45, Num 6, pp 774-776, issn 0148-7299Article

A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH)RAUCH, A; PFEIFFER, R. A; TRAUTMANN, U et al.Clinical genetics. 1992, Vol 42, Num 2, pp 84-90, issn 0009-9163Article

Characterization of seven DA/DAPI-positive bisatellitedc marker chromosomes by in situ hydridizationPLATTNER, R; HEEREMA, N. A; PATIL, S. R et al.Human genetics. 1991, Vol 87, Num 3, pp 290-296, issn 0340-6717Article