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Results:
1-7
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Results: 7
Authors:
SILLEN A
ALDERBORN A
PIGG M
JAGELL S
WADELIUS C
Citation: A. Sillen et al., DETAILED GENETIC AND PHYSICAL MAPPING IN THE SJOGREN-LARSSON-SYNDROMEGENE REGION IN 17P11.2, Hereditas, 128(3), 1998, pp. 245-250
Authors:
DAHL N
PIGG M
RISTOFF E
GALI R
CARLSSON B
MANNERVIK B
LARSSON A
BOARD P
Citation: N. Dahl et al., MISSENSE MUTATIONS IN THE HUMAN GLUTATHIONE SYNTHETASE GENE RESULT INSEVERE METABOLIC-ACIDOSIS, 5-OXOPROLINURIA, HEMOLYTIC-ANEMIA AND NEUROLOGICAL DYSFUNCTION, Human molecular genetics, 6(7), 1997, pp. 1147-1152
Authors:
PIGG M
GEDDEDAHL T
COX D
ANTONLAMPRECHT I
HAUSSER I
DAHL N
Citation: M. Pigg et al., FOUNDER EFFECT FOR A SPLICE-SITE MUTATION IN THE TRANSGLUTAMINASE-1 GENE IN CONGENITAL RECESSIVE ICHTHYOSIS TYPE-I AND TYPE-II IN NORWAY, American journal of human genetics, 61(4), 1997, pp. 2011-2011
Authors:
PIGG M
JAGELL S
SILLEN A
WEISSENBACH J
GUSTAVSON KH
WADELIUS C
Citation: M. Pigg et al., THE SJOGREN-LARSSON SYNDROME GENE IS CLOSE TO D17S805 AS DETERMINED BY LINKAGE ANALYSIS AND ALLELIC ASSOCIATION (VOL 8, PG 361, 1994), Nature genetics, 9(4), 1995, pp. 451-451
Authors:
AGARDI D
PIGG M
SJOHOLM AG
TRUEDSSON L
SPATH PJ
KUIJPER EJ
TIJSSEN CC
TRANEBJAERG L
GUSTAVSON KH
ULFENDAHL PJ
WADELIUS C
Citation: D. Agardi et al., FLUORESCENT DETECTION OF MICROSATELLITE POLYMORPHISMS - PROPERDIN DEFICIENCY LINKED TO PFC MICROSATELLITE, Experimental and clinical immunogenetics, 12(2), 1995, pp. 111-114
Authors:
ALDERBORN A
SILLEN A
PIGG M
JAGELL S
BRAUNQUENTIN C
WEISSENBACH J
GUSTAVSON KH
WADELIUS C
Citation: A. Alderborn et al., HIGH-RESOLUTION MAPPING OF SJOGREN-LARSSON SYNDROME - THE GENE IS LOCATED IN A 0 CM INTERVAL IN 17P11.2, American journal of human genetics, 57(4), 1995, pp. 1060-1060
Authors:
PIGG M
JAGELL S
SILLEN A
WEISSENBACH J
GUSTAVSON KH
WADELIUS C
Citation: M. Pigg et al., THE SJOGREN-LARSSON SYNDROME GENE IS CLOSE TO D17S805 AS DETERMINED BY LINKAGE ANALYSIS AND ALLELIC ASSOCIATION, Nature genetics, 8(4), 1994, pp. 361-364
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1-7
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