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ZIDAR J
EKICI A
PETERLLIN B
RAUTENSTRAUSS B
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Authors:
DITTRICH F
ZAJONC D
HUHNE K
HOJA U
EKICI A
GREINER E
KLEIN H
HOFMANN J
BESSOULE JJ
SPERLING P
SCHWEIZER E
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Authors:
LIEHR T
RAUTENSTRAUSS B
GREHL H
BATHKE KD
EKICI A
RAUCH A
ROTT HD
Citation: T. Liehr et al., MOSAICISM FOR THE CHARCOT-MARIE-TOOTH DISEASE TYPE 1A DUPLICATION SUGGESTS SOMATIC REVERSION, Human genetics, 98(1), 1996, pp. 22-28
Authors:
LIEHR T
EKICI A
HILLENBRAND R
RAUTENSTRAUSS B
Citation: T. Liehr et al., REGIONAL LOCALIZATION OF RAT MYELIN PROTEIN ZERO MPZ GENE TO CHROMOSOME 13Q24-25 BY MEANS OF FISH, Mammalian genome, 6(11), 1995, pp. 824-825
Authors:
BATHKE KD
LIEHR T
EKICI A
TIMMERMAN V
VANBROECKHOVEN C
GREHL H
NEUNDORFER B
RAUTENSTRAUSS B
Citation: Kd. Bathke et al., EVIDENCE FOR A MODIFIED RECOMBINATION EVENT IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (HNPP), American journal of human genetics, 57(4), 1995, pp. 1195-1195
Authors:
LIEHR T
EKICI A
HILLENBRAND R
SCHACHNER M
RAUTENSTRAUSS B
Citation: T. Liehr et al., ASSIGNMENT OF PMP22 AND PO, CANDIDATE GENES FOR CHARCOT-MARIE-TOOTH (CMT) DISEASE TYPE 1A AND 1B TO RAT CHR 10Q22 AND 13Q24-26 BY FISH, American journal of human genetics, 57(4), 1995, pp. 1888-1888
Authors:
RAUTENSTRAUSS B
GOTZ A
LIEHR T
GREHL H
SOSTARKO M
BATHKE KD
EKICI A
PARK O
DUMSER T
HAUSMANN R
HILLENBRAND R
SCHACHNER M
PFEIFFER RA
NEUNDORFER B
Citation: B. Rautenstrauss et al., MYELIN-ASSOCIATED GLYCOPROTEIN IMMUNOREACTIVITY AND CHARCOT-MARIE-TOOTH (CMT) DISEASE TYPE 1A - ASSOCIATION OF CMT AND MULTIPLE-SCLEROSIS, American journal of human genetics, 57(4), 1995, pp. 1975-1975