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Results: 1-6 |
Results: 6

Authors: KRAUS C BATHKE KD SILLEN A BALLHAUSEN WG PFEIFFER RA
Citation: C. Kraus et al., RNA BASED MUTATION SCREENING OF THE FALDH GENE IN GERMAN FAMILIES WITH SJOGREN-LARSSON-SYNDROME, European journal of human genetics, 6, 1998, pp. 4183-4183

Authors: TIMMERMAN V RAUTENSTRAUSS B REITER LT KOEUTH T LOFGREN A LIEHR T NELIS E BATHKE KD DEJONGHE P GREHL H MARTIN JJ LUPSKI JR VANBROECKHOVEN C
Citation: V. Timmerman et al., DETECTION OF THE CMT1A HNPP RECOMBINATION HOTSPOT IN UNRELATED PATIENTS OF EUROPEAN DESCENT/, Journal of Medical Genetics, 34(1), 1997, pp. 43-49

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: 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: 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

Authors: JARDINE PE KOCH MC LUNT P MAYNARD J BATHKE KD HARPER PS UPADHYAYA M
Citation: Pe. Jardine et al., DE-NOVO FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY DEFINED BY DNA-PROBE P13E-11 (D4F104S1), Archives of Disease in Childhood, 71(3), 1994, pp. 221-227
Risultati: 1-6 |