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Results:
1-13
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Results: 13
Authors:
GAUDENZ K
ROESSLER E
QUADERI N
FRANCO B
FELDMAN G
GASSER DL
WITTWER B
HORST J
MONTINI E
OPITZ JM
BALLABIO A
MUENKE M
Citation: K. Gaudenz et al., OPITZ G BBB SYNDROME IN XP22 - MUTATIONS IN THE MID1 GENE-CLUSTER IN THE CARBOXY-TERMINAL DOMAIN (VOL 63, PG 703, 1998)/, American journal of human genetics, 63(5), 1998, pp. 1571-1571
Authors:
GAUDENZ K
ROESSLER E
QUADERI N
FRANCO B
FELDMAN G
GASSER DL
WITTWER B
MONTINI E
OPITZ JM
BALLABIO A
MUENKE M
Citation: K. Gaudenz et al., OPITZ G BBB SYNDROME IN XP22 - MUTATIONS IN THE MID1 GENE-CLUSTER IN THE CARBOXY-TERMINAL DOMAIN/, American journal of human genetics, 63(3), 1998, pp. 703-710
Authors:
WITTWER B
EXELER R
BUCHTER D
HORST J
Citation: B. Wittwer et al., A BOY WITH 47,XY,-15)(Q32-Q13)MAT RESULTING FROM A SEGREGATIONAL TYPE-3(DER(15)T(1)1 - A CLINICAL CHARACTERIZATION/, American journal of human genetics, 61(4), 1997, pp. 817-817
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:
RABE H
BRUNE T
ROSSI R
STEINHORST V
JORCH G
HORST J
WITTWER B
Citation: H. Rabe et al., YUNIS-VARON SYNDROME - THE FIRST CASE OF GERMAN ORIGIN, Clinical dysmorphology, 5(3), 1996, pp. 217-222
Authors:
WITTWER B
KIRCHEISEN R
LEUTELT J
ORTH U
GAL A
Citation: B. Wittwer et al., NEW X-LINKED MENTAL-RETARDATION SYNDROME WITH THE GENE MAPPED TENTATIVELY IN XP22.3, American journal of medical genetics, 64(1), 1996, pp. 42-49
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
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:
WITTWER B
PALM DG
SCHUIERER G
HORST J
Citation: B. Wittwer et al., POLYMICROGYRIA IN 2 BROTHERS - EVIDENCE FOR AN INHERITED NEURONAL MIGRATION DISORDER, American journal of human genetics, 57(4), 1995, pp. 506-506
Authors:
CARVALHO MRS
MEINDL A
STROM TM
MULLER B
WITTWER B
ROSS M
MEITINGER T
Citation: Mrs. Carvalho et al., X-CHROMOSOMAL RETINITIS-PIGMENTOSA - GENETIC-MAPPING AND CLONING APPROACHES, Cytogenetics and cell genetics, 67(4), 1994, pp. 343-343
Authors:
CARVALHO MRS
MEINDL A
STROM T
MULLER B
WITTWER B
ROSS M
MEITINGER T
Citation: Mrs. Carvalho et al., X-CHROMOSOMAL RETINITIS-PIGMENTOSA - GENETIC-MAPPING AND CLONING APPROACHES, American journal of human genetics, 53(3), 1993, pp. 1068-1068
Authors:
WITTWER B
ZYGULSKA M
MINY P
EIGEL A
HORST J
Citation: B. Wittwer et al., TESTING FOR FRAGILE X-SYNDROME IN 120 FAMILIES WITH A HISTORY OF MENTAL-RETARDATION, American journal of human genetics, 53(3), 1993, pp. 1513-1513
Authors:
ZYGULSKA M
MILEWSKI M
WITTWER B
EIGEL A
BAL J
MAZURCZAK T
HORST J
Citation: M. Zygulska et al., ANALYSIS OF FMR-1-GENE MUTATIONS IN 16 POLISH FAMILIES WITH FRA-X SYNDROME, American journal of human genetics, 53(3), 1993, pp. 1769-1769
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