Citation: Br. Migeon et C. Haisleyroyster, FAMILIAL SKEWED X INACTIVATION AND X-LINKED MUTATIONS - UNBALANCED X INACTIVATION IS A POWERFUL MEANS TO ASCERTAIN X-LINKED GENES THAT AFFECT CELL-PROLIFERATION, American journal of human genetics, 62(6), 1998, pp. 1555-1557
Citation: Ay. Liu et al., THE HUMAN NTT GENE - IDENTIFICATION OF A NOVEL 17-KB NONCODING NUCLEAR-RNA EXPRESSED IN ACTIVATED CD4(-CELLS() T), Genomics, 39(2), 1997, pp. 171-184
Authors:
MIGEON BR
JEPPESEN P
TORCHIA BS
FU SD
DUNN MA
AXELMAN J
SCHMECKPEPER BJ
FANTES J
ZORI RT
DRISCOLL DJ
Citation: Br. Migeon et al., LACK OF X INACTIVATION ASSOCIATED WITH MATERNAL X ISODISOMY - EVIDENCE FOR A COUNTING MECHANISM PRIOR TO X INACTIVATION DURING HUMAN EMBRYOGENESIS, American journal of human genetics, 58(1), 1996, pp. 161-170
Citation: Mm. Jani et al., MOLECULAR CHARACTERIZATION OF TINY RING X-CHROMOSOMES FROM FEMALES WITH FUNCTIONAL X-CHROMOSOME DISOMY AND LACK OF CIS-X INACTIVATION, Genomics, 27(1), 1995, pp. 182-188
Citation: Bs. Torchia et Br. Migeon, THE XIST LOCUS REPLICATES LATE ON THE ACTIVE-X, AND EARLIER ON THE INACTIVE-X BASED ON FISH DNA-REPLICATION ANALYSIS OF SOMATIC-CELL HYBRIDS, Somatic cell and molecular genetics, 21(5), 1995, pp. 327-333
Authors:
MIGEON BR
STETTEN G
TUCKMULLER C
AXELMAN J
JANI M
DUNGY D
Citation: Br. Migeon et al., MOLECULAR CHARACTERIZATION OF A DELETED X-CHROMOSOME (XQ13.3-XQ21.31)EXHIBITING RANDOM X-INACTIVATION, Somatic cell and molecular genetics, 21(2), 1995, pp. 113-120
Citation: Sy. Luo et al., XIST EXPRESSION IS REPRESSED WHEN X INACTIVATION IS REVERSED IN HUMANPLACENTAL CELLS - A MODEL FOR STUDY OF XIST REGULATION, Somatic cell and molecular genetics, 21(1), 1995, pp. 51-60
Citation: Bs. Torchia et al., REPLICATION ANALYSIS OF X-LINKED GENES IN FEMALES BY FLUORESCENCE IN-SITU HYBRIDIZATION (FISH), Cytogenetics and cell genetics, 69(1-2), 1995, pp. 122-122
Authors:
MIGEON BR
DUNN MA
THOMAS G
SCHMECKPEPER BJ
NAIDU S
Citation: Br. Migeon et al., STUDIES OF X-INACTIVATION AND ISODISOMY IN TWINS PROVIDE FURTHER EVIDENCE THAT THE X-CHROMOSOME IS NOT INVOLVED IN RETT-SYNDROME, American journal of human genetics, 56(3), 1995, pp. 647-653
Citation: M. Jani et al., DELETION MAPPING OF 7 ABNORMAL X-CHROMOSOMES REVEALS BREAKPOINTS AND LOCALIZES 3 MICROSATELLITE MARKERS, Cytogenetics and cell genetics, 67(4), 1994, pp. 343-344
Citation: Br. Migeon et al., THE SEVERE PHENOTYPE OF FEMALES WITH TINY RING X-CHROMOSOMES IS ASSOCIATED WITH INABILITY OF THESE CHROMOSOMES TO UNDERGO X-INACTIVATION, American journal of human genetics, 55(3), 1994, pp. 497-504
Citation: Bs. Torchia et al., DNA-REPLICATION ANALYSIS OF FMRI, XIST, AND FACTOR 8C LOCI BY FISH SHOWS NONTRANSCRIBED X-LINKED GENES REPLICATE LATE, American journal of human genetics, 55(1), 1994, pp. 96-104
Authors:
MIGEON BR
MCGINNISS MJ
ANTONARAKIS SE
AXELMAN J
STASIOWSKI BA
YOUSSOUFIAN H
KEARNS WG
CHUNG A
PEARSON PL
KAZAZIAN HH
MUNEER RS
Citation: Br. Migeon et al., SEVERE HEMOPHILIA-A IN A FEMALE BY CRYPTIC TRANSLOCATION - ORDER AND ORIENTATION OF FACTOR-VIII WITHIN XQ28 (VOL 16, PG 20, 1993), Genomics, 16(3), 1993, pp. 792-792
Citation: Sy. Luo et al., DNA METHYLATION OF THE FRAGILE-X LOCUS IN SOMATIC AND GERM-CELLS DURING FETAL DEVELOPMENT - RELEVANCE TO THE FRAGILE-X SYNDROME AND X-INACTIVATION, Somatic cell and molecular genetics, 19(4), 1993, pp. 393-404
Citation: Ba. Stasiowski et Br. Migeon, RESOLUTION OF LOCI 600 KB APART BY FLUORESCENCE IN-SITU HYBRIDIZATIONTO METAPHASE CHROMOSOMES, Cytogenetics and cell genetics, 64(3-4), 1993, pp. 181-182
Citation: Br. Migeon, ROLE OF DNA METHYLATION IN X-INACTIVATION AND THE FRAGILE X-SYNDROME, American journal of medical genetics, 46(6), 1993, pp. 685-686
Authors:
MIGEON BR
LUO SY
STASIOWSKI BA
JANI M
AXELMAN J
VANDYKE DL
WEISS L
JACOBS PA
YANGFENG TL
WILEY JE
Citation: Br. Migeon et al., DEFICIENT TRANSCRIPTION OF XIST FROM TINY RING X-CHROMOSOMES IN FEMALES WITH SEVERE PHENOTYPES, Proceedings of the National Academy of Sciences of the United Statesof America, 90(24), 1993, pp. 12025-12029
Citation: Lm. Call et Br. Migeon, DNA-REPLICATION ANALYSIS OF X-LINKED FMR-1, XIST AND FACTOR-8C LOCI USING FLUORESCENCE IN-SITU HYBRIDIZATION INDICATES NONTRANSCRIBED GENESARE LATE REPLICATING, American journal of human genetics, 53(3), 1993, pp. 224-224
Authors:
MIGEON BR
LUO S
STASIOWSKI BA
JANI M
AXELMAN J
VANDYKE DL
WEISS L
JACOBS PA
YANGFENG TL
WILEY JE
Citation: Br. Migeon et al., DEFICIENT TRANSCRIPTION OF XIST IN FEMALES WITH TINY RING X-CHROMOSOMES AND SEVERE PHENOTYPES - IMPLICATIONS FOR THE ROLE OF XIST IN X-INACTIVATION, American journal of human genetics, 53(3), 1993, pp. 226-226