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Results:
1-10
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Results: 10
Authors:
COFFEY AJ
BROOKSBANK RA
BRANDAU O
OOHASHI T
HOWELL GR
BYE JM
CAHN AP
DURHAM J
HEATH P
WRAY P
PAVITT R
WILKINSON J
LEVERSHA M
HUCKLE E
SHAWSMITH CJ
DUNHAM A
RHODES S
SCHUSTER V
PORTA G
YIN L
SERAFINI P
SYLLA B
ZOLLO M
FRANCO B
BOLINO A
SERI M
LANYI A
DAVIS JR
WEBSTER D
HARRIS A
LENOIR G
STBASILE GD
JONES A
BEHLORADSKY BH
ACHATZ H
MURKEN J
FASSLER R
SUMEGI J
ROMEO G
VAUDIN M
ROSS MT
MEINDL A
BENTLEY DR
Citation: Aj. Coffey et al., HOST RESPONSE TO EBV INFECTION IN X-LINKED LYMPHOPROLIFERATIVE DISEASE RESULTS FROM MUTATIONS IN AN SH2-DOMAIN ENCODING GENE, Nature genetics, 20(2), 1998, pp. 129-135
Authors:
BRANDAU O
NYAKATURA G
JEDELE KB
PLATZER M
ACHATZ H
ROSS M
MURKEN J
ROSENTHAL A
MEINDL A
Citation: O. Brandau et al., UHX1 AND PCTK1 - PRECISE CHARACTERIZATION AND LOCALIZATION WITHIN A GENE-RICH REGION IN XP11.23 AND EVALUATION AS CANDIDATE GENES FOR RETINAL DISEASES MAPPED TO XP21.1-P11.2, European journal of human genetics, 6(5), 1998, pp. 459-466
Authors:
MEINDL A
BRANDAU O
NYAKATURA G
ACHATZ H
HELLEBRAND H
RAMSER J
ROSS M
ROSENTHAL A
Citation: A. Meindl et al., SCREENING FOR FURTHER XLRP GENES IN SEQUENCE READY MAPS FROM XP21.1 AND XP11.23, European journal of human genetics, 6, 1998, pp. 4174-4174
Authors:
MEINDL A
DRY K
HERRMANN K
MANSON F
CICCODICOLA A
EDGAR A
CARVALHO MRS
ACHATZ H
HELLEBRAND H
LENNON A
MIGLIACCIO C
PORTER K
ZRENNER E
BIRD A
JAY M
LORENZ B
WITTWER B
DURSO M
MEITINGER T
WRIGHT A
Citation: A. Meindl et al., A GENE (RPGR) WITH HOMOLOGY TO THE RCC1 GUANINE-NUCLEOTIDE EXCHANGE FACTOR IS MUTATED IN X-LINKED RETINITIS-PIGMENTOSA (RP3), Nature genetics, 13(1), 1996, pp. 35-42
Authors:
ZRENNER E
LORENZ B
WITTWER B
APFELSTEDT E
WISSINGER B
HERGERSBERG M
RUDOLPH G
HERRMANN K
ACHATZ H
MEINDL A
MEITINGER T
Citation: E. Zrenner et al., MUTATION ANALYSIS IN PATIENTS WITH X-LINKED RETINITIS-PIGMENTOSA, Vision research, 36, 1996, pp. 3231-3231
Authors:
MEINDL A
LORENZ B
ACHATZ H
HELLEBRAND H
SCHMITZVALCKENBERG P
MEITINGER T
Citation: A. Meindl et al., MISSENSE MUTATIONS IN THE NDP GENE IN PATIENTS WITH A LESS SEVERE COURSE OF NORRIE DISEASE, Human molecular genetics, 4(3), 1995, pp. 489-490
Authors:
MEINDL A
CARVALHO MRS
HERRMANN K
LORENZ B
ACHATZ H
LORENZ B
APFELSTEDTSYLLA E
WITTWER B
ROSS M
MEITINGER T
Citation: A. Meindl et al., A GENE (SRPX) ENCODING A SUSHI-REPEAT-CONTAINING PROTEIN IS DELETED IN PATIENTS WITH X-LINKED RETINITIS-PIGMENTOSA, Human molecular genetics, 4(12), 1995, pp. 2339-2346
Authors:
MEINDL A
CARVALHO MRS
LORENZ B
ACHATZ H
HERRMANN K
LICHTNER P
ROSS M
MEITINGER T
Citation: A. Meindl et al., CLONING OF CANDIDATE GENES FOR X-LINKED RETINITIS-PIGMENTOSA, American journal of human genetics, 57(4), 1995, pp. 1537-1537
Authors:
DEUFEL A
DEUFEL T
GOLLA A
ACHATZ H
BERTELEHARMS R
ROSCHER AA
MEITINGER T
Citation: A. Deufel et al., 3 NOVEL MUTATIONS (I506S, S466X, 1651A-]T) IN EXON-10 OF THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR (CFTR) DETECTED IN PATIENTS OF SOUTHERN GERMAN DESCENT, Human mutation, 3(1), 1994, pp. 64-66
Authors:
SCHINDELHAUER D
ACHATZ H
STROM TM
ROSS M
CARVALHO MRS
MEINDL A
Citation: D. Schindelhauer et al., ISOLATION AND FINE MAPPING OF (CA)(N) REPEATS FROM THE XP11.23 AND XP11.4 REGION, Human molecular genetics, 3(6), 1994, pp. 1027-1027
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1-10
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