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