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Results: 1-8 |
Results: 8
A GENE FOR FG-SYNDROME MAPS IN THE XQ12-Q21.31 REGION
Authors: BRIAULT S HILL R SHRIMPTON A ZHU DP TILL M RONCE N MARGARITTEJEANNIN P BARAITSER M MIDDLETONPRICE H MALCOLM S THOMPSON E HOO J WILSON G ROMANO C GUICHET A PEMBREY M FONTES M POUSTKA A MORAINE C
Citation: S. Briault et al., A GENE FOR FG-SYNDROME MAPS IN THE XQ12-Q21.31 REGION, American journal of medical genetics, 73(1), 1997, pp. 87-90
MUTATIONS IN THE X-LINKED AND AUTOSOMAL RECESSIVE FORMS OF CHRONIC GRANULOMATOUS-DISEASE
Authors: ROOS D DEBOER M KURIBAYASHI F MEISCHL C WEENING RS SEGAL AW AHLIN A NEMET K HOSSLE JP BERNATOWSKAMATUSZKIEWICZ E MIDDLETONPRICE H
Citation: D. Roos et al., MUTATIONS IN THE X-LINKED AND AUTOSOMAL RECESSIVE FORMS OF CHRONIC GRANULOMATOUS-DISEASE, Blood, 87(5), 1996, pp. 1663-1681
MEIOTIC DRIVE AND MYOTONIC-DYSTROPHY - REPLY
Authors: CAREY N JOHNSON K NOKELAINEN P PELTONEN L SAVONTAUS ML JUVONEN V ANVRET M GRANDELL U CHOTAI K ROBERTSON E MIDDLETONPRICE H MALCOLM S
Citation: N. Carey et al., MEIOTIC DRIVE AND MYOTONIC-DYSTROPHY - REPLY, Nature genetics, 10(2), 1995, pp. 133-133
CYSTIC-FIBROSIS MUTATION ANALYSIS - REPORT FROM 22 UK REGIONAL GENETICS LABORATORIES
Authors: SCHWARZ MJ MALONE GM HAWORTH A CHEADLE JP MEREDITH AL GARDNER A SAWYER IH CONNARTY M DENNIS N SELLER A HARRIS A TAYLOR R DEAR S MIDDLETONPRICE H MCMAHON C MAYALL E MCMAHON R BARTON DE GILES M LINDLEY V PLAHA DS PRICE S SHARIF A CROSS GS DALTON A TAYLOR G WALLACE A TASSABEHJI M WHITTAKER JL BUTLER R CURTIS A PINKETT R GILFILLAN AJ BROCK DJH HIGGINS GS LANYON G MIEDZYBRODZKA Z DAVIDSON M GRAHAM CA HILL AJM
Citation: Mj. Schwarz et al., CYSTIC-FIBROSIS MUTATION ANALYSIS - REPORT FROM 22 UK REGIONAL GENETICS LABORATORIES, Human mutation, 6(4), 1995, pp. 326-333
MEIOTIC DRIVE AT THE MYOTONIC-DYSTROPHY LOCUS
Authors: CAREY N JOHNSON K NOKELAINEN P PELTONEN L SAVONTAUS ML JUVONEN V ANVRET M GRANDELL U CHOTAI K ROBERTSON E MIDDLETONPRICE H MALCOLM S
Citation: N. Carey et al., MEIOTIC DRIVE AT THE MYOTONIC-DYSTROPHY LOCUS, Nature genetics, 6(2), 1994, pp. 117-118
NORRIE DISEASE GENE - CHARACTERIZATION OF DELETIONS AND POSSIBLE FUNCTION
Authors: CHEN ZY BATTINELLI EM HENDRIKS RW POWELL JF MIDDLETONPRICE H SIMS KB BREAKEFIELD XO CRAIG IW
Citation: Zy. Chen et al., NORRIE DISEASE GENE - CHARACTERIZATION OF DELETIONS AND POSSIBLE FUNCTION, Genomics, 16(2), 1993, pp. 533-535
A NEW RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM AT THE DXS101 LOCUS ALLOWS CARRIER DETECTION IN A FAMILY WITH X-LINKED AGAMMAGLOBULINEMIA
Authors: SWEATMAN A LOVERING R MIDDLETONPRICE H JONES A MORGAN G LEVINSKY R KINNON C
Citation: A. Sweatman et al., A NEW RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM AT THE DXS101 LOCUS ALLOWS CARRIER DETECTION IN A FAMILY WITH X-LINKED AGAMMAGLOBULINEMIA, Journal of Medical Genetics, 30(6), 1993, pp. 512-514
CARRIER DETERMINATION FOR X-LINKED AGAMMAGLOBULINEMIA USING X-INACTIVATION ANALYSIS OF PURIFIED B-CELLS
Authors: ALTERMAN LA DEALWIS M GENET S LOVERING R MIDDLETONPRICE H MORGAN G JONES A MALCOLM S LEVINSKY RJ KINNON C
Citation: La. Alterman et al., CARRIER DETERMINATION FOR X-LINKED AGAMMAGLOBULINEMIA USING X-INACTIVATION ANALYSIS OF PURIFIED B-CELLS, Journal of immunological methods, 166(1), 1993, pp. 111-116
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