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Authors: GUNTER C PARADEE W CRAWFORD DC MEADOWS KA NEWMAN J KUNST CB NELSON DL SCHWARTZ C MURRAY A MACPHERSON JN SHERMAN SL WARREN ST
Citation: C. Gunter et al., REEXAMINATION OF FACTORS ASSOCIATED WITH EXPANSION OF CGG REPEATS USING A SINGLE NUCLEOTIDE POLYMORPHISM IN FMR1, Human molecular genetics (Print), 7(12), 1998, pp. 1935-1946

Authors: SMALL K WARREN ST
Citation: K. Small et St. Warren, EMERIN DELETIONS OCCURRING ON BOTH XQ28 INVERSION BACKGROUNDS, Human molecular genetics, 7(1), 1998, pp. 135-139

Authors: GUNTER C WARREN ST
Citation: C. Gunter et St. Warren, POLYMORPHISM IN THE FMR1 GENE, Human genetics, 103(3), 1998, pp. 365-365

Authors: CHOU HH TAKEMATSU H DIAZ S IBER J NICKERSON E WRIGHT KL MUCHMORE EA NELSON DL WARREN ST VARKI A
Citation: Hh. Chou et al., A MUTATION IN HUMAN CMP-SIALIC ACID HYDROXYLASE OCCURRED AFTER THE HOMO-PAN DIVERGENCE, Proceedings of the National Academy of Sciences of the United Statesof America, 95(20), 1998, pp. 11751-11756

Authors: BROWN V SMALL K LAKKIS L FENG Y GUNTER C WILKINSON KD WARREN ST
Citation: V. Brown et al., PURIFIED RECOMBINANT FMRP EXHIBITS SELECTIVE RNA-BINDING AS AN INTRINSIC PROPERTY OF THE FRAGILE-X MENTAL-RETARDATION PROTEIN, The Journal of biological chemistry, 273(25), 1998, pp. 15521-15527

Authors: ZABAWA RE WARREN ST
Citation: Re. Zabawa et St. Warren, FROM COMPANY TO COMMUNITY - AGRICULTURAL COMMUNITY-DEVELOPMENT IN MACON COUNTY, ALABAMA, 1881 TO THE NEW-DEAL, Agricultural history, 72(2), 1998, pp. 459-486

Authors: WARREN ST ZABAWA RE
Citation: St. Warren et Re. Zabawa, THE ORIGINS OF THE TUSKEGEE NATIONAL FOREST - 19TH-CENTURY AND 20TH-CENTURY RESETTLEMENT AND LAND-DEVELOPMENT PROGRAMS IN THE BLACK-BELT REGION OF ALABAMA, Agricultural history, 72(2), 1998, pp. 487-508

Authors: WARREN ST
Citation: St. Warren, TRINUCLEOTIDE REPETITION AND FRAGILE-X-SYNDROME, Hospital practice, 32(4), 1997, pp. 73

Authors: FENG Y ABSHER D EBERHART DE BROWN V MALTER HE WARREN ST
Citation: Y. Feng et al., FMRP ASSOCIATES WITH POLYRIBOSOMES AS AN MRNP, AND THE I304N MUTATIONOF SEVERE FRAGILE-X-SYNDROME ABOLISHES THIS ASSOCIATION, MOLECULAR CELL, 1(1), 1997, pp. 109-118

Authors: SMALL K IBER J WARREN ST
Citation: K. Small et al., EMERIN DELETION REVEALS A COMMON X-CHROMOSOME INVERSION MEDIATED BY INVERTED REPEATS, Nature genetics, 16(1), 1997, pp. 96-99

Authors: MALTER HE IBER JC WILLEMSEN R DEGRAAFF E TARLETON JC LEISTI J WARREN ST OOSTRA BA
Citation: He. Malter et al., CHARACTERIZATION OF THE FULL FRAGILE-X-SYNDROME MUTATION IN FETAL GAMETES, Nature genetics, 15(2), 1997, pp. 165-169

Authors: SMALL K WAGENER M WARREN ST
Citation: K. Small et al., ISOLATION AND CHARACTERIZATION OF THE COMPLETE MOUSE EMERIN GENE, Mammalian genome, 8(5), 1997, pp. 337-341

Authors: FENG Y GUTEKUNST CA EBERHART DE YI H WARREN ST HERSCH SM
Citation: Y. Feng et al., FRAGILE-X MENTAL-RETARDATION PROTEIN - NUCLEOCYTOPLASMIC SHUTTLING AND ASSOCIATION WITH SOMATODENDRITIC RIBOSOMES, The Journal of neuroscience, 17(5), 1997, pp. 1539-1547

Authors: WARREN ST
Citation: St. Warren, POLYALANINE EXPANSION IN SYNPOLYDACTYLY MIGHT RESULT FROM UNEQUAL CROSSING-OVER OF HOXD13, Science, 275(5298), 1997, pp. 408-409

Authors: KUNST CB LEEFLANG EP IBER JC ARNHEIM N WARREN ST
Citation: Cb. Kunst et al., THE EFFECT OF FMR1 CGG REPEAT INTERRUPTIONS ON MUTATION FREQUENCY AS MEASURED BY SPERM TYPING, Journal of Medical Genetics, 34(8), 1997, pp. 627-631

Authors: LOSEKOOT M HOOGENDOORN E OLMER R JANSEN CCAM OOSTERWIJK JC VANDENOUWELAND AMW HALLEY DJJ WARREN ST WILLEMSEN R OOSTRA BA BAKKER E
Citation: M. Losekoot et al., PRENATAL-DIAGNOSIS OF THE FRAGILE-X-SYNDROME - LOSS OF MUTATION OWINGTO A DOUBLE RECOMBINANT OR GENE CONVERSION EVENT AT THE FMR1 LOCUS, Journal of Medical Genetics, 34(11), 1997, pp. 924-926

Authors: KENNESON A CRAMER DW WARREN ST
Citation: A. Kenneson et al., FRAGILE-X PREMUTATIONS ARE NOT A MAJOR CAUSE OF EARLY MENOPAUSE, American journal of human genetics, 61(6), 1997, pp. 1362-1369

Authors: KENNESON A CRAMER DW WARREN ST
Citation: A. Kenneson et al., THE FRAGILE-X PREMUTATION IS NOT A MAJOR RISK FOR EARLY MENOPAUSE, American journal of human genetics, 61(4), 1997, pp. 19-19

Authors: WINKELER KA LAKKIS L WARREN ST
Citation: Ka. Winkeler et al., DIFFERENTIATION OF PC12 CELLS RESULTS IN ALTERNATIVE SPLICING CHANGESIN THE FMR1 GENE LEADING TO HIGH EXPRESSION OF ISOFORM-4, American journal of human genetics, 61(4), 1997, pp. 128-128

Authors: BROWN VL SMALL K LAKKIS L WILKINSON KD WARREN ST
Citation: Vl. Brown et al., PURIFICATION AND CHARACTERIZATION OF THE FRAGILE-X MENTAL-RETARDATIONPROTEIN, American journal of human genetics, 61(4), 1997, pp. 132-132

Authors: GUNTER C PARADEE W NEWMAN J SHERMAN SL WARREN ST
Citation: C. Gunter et al., A NOVEL BIALLELIC POLYMORPHISM IN THE FMR1 GENE SHOWS STRONG LINKAGE DISEQUILIBRIUM WITH CGG REPEATS AND FLANKING MICROSATELLITE MARKERS, American journal of human genetics, 61(4), 1997, pp. 152-152

Authors: PARADEE W RASMUSSEN D MELIKIAN H CONN PJ WARREN ST
Citation: W. Paradee et al., HIPPOCAMPUS-INDEPENDENT DEFICITS IN THE FRAGILE-X MOUSE, American journal of human genetics, 61(4), 1997, pp. 916-916

Authors: FENG Y ABSHER D BROWN V EBERHART DE MALTER HE WARREN ST
Citation: Y. Feng et al., FMRP ASSOCIATES WITH POLYRIBOSOMES AS AN MRNP AND THE I304N MUTATION CAUSING SEVERE FRAGILE-X-SYNDROME ABOLISHES THIS ASSOCIATION, American journal of human genetics, 61(4), 1997, pp. 976-976

Authors: SMALL K WAGENER M WARREN ST
Citation: K. Small et al., COMPLETE EMERIN DELETIONS LEADING TO EMERY-DREIFUSS MUSCULAR-DYSTROPHY OCCUR ON COMMON XQ28 INVERSION BACKGROUNDS, American journal of human genetics, 61(4), 1997, pp. 1057-1057

Authors: LINDBLAD K BURGESS CE YUAN QP LAKKIS L HUDSON TJ WARREN ST SCHALLING M
Citation: K. Lindblad et al., A STRATEGY FOR IDENTIFICATION OF SEQUENCE FLANKING TRINUCLEOTIDE REPEAT EXPANSION LOCI, American journal of human genetics, 61(4), 1997, pp. 1832-1832
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