Citation: Ee. Eichler et al., COMPLEX BETA-SATELLITE REPEAT STRUCTURES AND THE EXPANSION OF THE ZINC-FINGER GENE-CLUSTER IN 19P12, PCR methods and applications, 8(8), 1998, pp. 791-808
Citation: Ee. Eichler, MASQUERADING REPEATS - PARALOGOUS PITFALLS OF THE HUMAN GENOME (VOL 8, PG 758, 1998), PCR methods and applications, 8(10), 1998, pp. 1095-1095
Authors:
HER C
WOOD TC
EICHLER EE
MOHRENWEISER HW
RAMAGLI LS
SICILIANO MJ
WEINSHILBOUM RM
Citation: C. Her et al., HUMAN HYDROXYSTEROID SULFOTRANSFERASE SULT2B1 - 2 ENZYMES ENCODED BY A SINGLE CHROMOSOME-19 GENE, Genomics (San Diego, Calif.), 53(3), 1998, pp. 284-295
Authors:
PEARSON CE
EICHLER EE
LORENZETTI D
KRAMER SF
ZOGHBI HY
NELSON DL
SINDEN RR
Citation: Ce. Pearson et al., INTERRUPTIONS IN THE TRIPLET REPEATS OF SCA1 AND FRAXA REDUCE THE PROPENSITY AND COMPLEXITY OF SLIPPED STRAND DNA (S-DNA) FORMATION, Biochemistry, 37(8), 1998, pp. 2701-2708
Authors:
EICHLER EE
BUDARF ML
ROCCHI M
DEAVEN LL
DOGGETT NA
BALDINI A
NELSON DL
MOHRENWEISER HW
Citation: Ee. Eichler et al., INTERCHROMOSOMAL DUPLICATIONS OF THE ADRENOLEUKODYSTROPHY LOCUS - A PHENOMENON OF PERICENTROMERIC PLASTICITY, Human molecular genetics, 6(7), 1997, pp. 991-1002
Authors:
FALIKZACCAI TC
SHACHAK E
YALON M
LIS Z
BOROCHOWITZ Z
MACPHERSON JN
NELSON DL
EICHLER EE
Citation: Tc. Falikzaccai et al., PREDISPOSITION TO THE FRAGILE-X-SYNDROME IN JEWS OF TUNISIAN DESCENT IS DUE TO THE ABSENCE OF AGG INTERRUPTIONS ON A RARE MEDITERRANEAN HAPLOTYPE, American journal of human genetics, 60(1), 1997, pp. 103-112
Authors:
EICHLER EE
LU F
SHEN Y
ANTONACCI R
JURECIC V
DOGGETT NA
MOYZIS RK
BALDINI A
GIBBS RA
NELSON DL
Citation: Ee. Eichler et al., DUPLICATION OF A GENE-RICH CLUSTER BETWEEN 16P11.1 AND XQ28 - A NOVELPERICENTROMERIC-DIRECTED MECHANISM FOR PARALOGOUS GENOME EVOLUTION, Human molecular genetics, 5(7), 1996, pp. 899-912
Authors:
EICHLER EE
MACPHERSON JN
MURRAY A
JACOBS PA
CHAKRAVARTI A
NELSON DL
Citation: Ee. Eichler et al., HAPLOTYPE AND INTERSPERSION ANALYSIS OF THE FMR1 CGG REPEAT IDENTIFIES 2 DIFFERENT MUTATIONAL PATHWAYS FOR THE ORIGIN OF THE FRAGILE-X SYNDROME, Human molecular genetics, 5(3), 1996, pp. 319-330
Citation: Ee. Eichler et Dl. Nelson, GENETIC-VARIATION AND EVOLUTIONARY STABILITY OF THE FMR1-CGG-REPEAT IN 6 CLOSED HUMAN-POPULATIONS, American journal of medical genetics, 64(1), 1996, pp. 220-225
Authors:
EICHLER EE
HAMMOND HA
MACPHERSON JN
WARD PA
NELSON DL
Citation: Ee. Eichler et al., POPULATION SURVEY OF THE HUMAN FMR1 CGG REPEAT SUBSTRUCTURE SUGGESTS BIASED POLARITY FOR THE LOSS OF AGG INTERRUPTIONS, Human molecular genetics, 4(12), 1995, pp. 2199-2208
Authors:
CHASTAIN PD
EICHLER EE
KANG S
NELSON DL
LEVENE SD
SINDEN RR
Citation: Pd. Chastain et al., ANOMALOUS RAPID ELECTROPHORETIC MOBILITY OF DNA CONTAINING TRIPLET REPEATS ASSOCIATED WITH HUMAN-DISEASE GENES, Biochemistry, 34(49), 1995, pp. 16125-16131
Authors:
EICHLER EE
LU F
ANTONACCI R
DOGGETT NA
MOYZIS RK
BALDINI A
GIBBS RA
NELSON DL
Citation: Ee. Eichler et al., TRANSPOSITION OF A GENE-CLUSTER FROM XQ28 TO 16P11.1 - A PERICENTROMERIC-DIRECTED MECHANISM FOR GENOME EVOLUTION, American journal of human genetics, 57(4), 1995, pp. 86-86
Authors:
FALIKBORENSTEIN TC
YALON M
SHACHAK L
DAR C
BOROCHOWITZ Z
NELSON DL
MACPHERSON JN
EICHLER EE
Citation: Tc. Falikborenstein et al., LONG UNINTERRUPTED CGG REPEATS WITHIN THE FMR1 GENE - POSSIBLE MECHANISM FOR THE PREVALENCE OF THE FRAGILE-X SYNDROME AMONG TUNISIAN JEWS, American journal of human genetics, 57(4), 1995, pp. 1218-1218
Citation: Ss. Chong et al., ROBUST AMPLIFICATION AND ETHIDIUM-VISIBLE DETECTION OF THE FRAGILE-X-SYNDROME CGG REPEAT USING PFU POLYMERASE, American journal of medical genetics, 51(4), 1994, pp. 522-526
Authors:
ASHLEY CT
SUTCLIFFE JS
KUNST CB
LEINER HA
EICHLER EE
NELSON DL
WARREN ST
Citation: Ct. Ashley et al., HUMAN AND MURINE FMR-1 - ALTERNATIVE SPLICING AND TRANSLATIONAL INITIATION DOWNSTREAM OF THE CGG-REPEAT, Nature genetics, 4(3), 1993, pp. 244-251
Authors:
VERKERK AJMH
DEGRAAFF E
DEBOULLE K
EICHLER EE
KONECKI DS
REYNIERS E
MANCA A
POUSTKA A
WILLEMS PJ
NELSON DL
OOSTRA BA
Citation: Ajmh. Verkerk et al., ALTERNATIVE SPLICING IN THE FRAGILE X-GENE FMR1 (VOL 2, PG 399, 1993), Human molecular genetics, 2(8), 1993, pp. 1348-1348