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Results: 1-20 |
Results: 20
A SUSCEPTIBILITY LOCUS FOR PARKINSONS-DISEASE MAPS TO CHROMOSOME 2P13
Authors: GASSER T MULLERMYHSOK B WSZOLEK ZK OEHLMANN R CALNE DB BONIFATI V BEREZNAI B FABRIZIO E VIEREGGE P HORSTMANN RD
Citation: T. Gasser et al., A SUSCEPTIBILITY LOCUS FOR PARKINSONS-DISEASE MAPS TO CHROMOSOME 2P13, Nature genetics, 18(3), 1998, pp. 262-265
A LINKAGE STUDY OF SPELLING DISORDER ON CHROMOSOME-1, CHROMOSOME-6, AND CHROMOSOME-15
Authors: SCHULTEKORNE G NOTHEN MM CICHON S GRIMM T MULLERMYHSOK B PROPPING P REMSCHMIDT H
Citation: G. Schultekorne et al., A LINKAGE STUDY OF SPELLING DISORDER ON CHROMOSOME-1, CHROMOSOME-6, AND CHROMOSOME-15, American journal of medical genetics, 81(6), 1998, pp. 459-459
APPROACHES TO THE GENETICS OF CARDIOVASCULAR-DISEASE THROUGH GENETIC FIELD WORK
Authors: SCHUSTER H LAMPRECHT A JUNGHANS C DIETZ B BARON H NOTHNAGEL M MULLERMYHSOK B LUFT FC
Citation: H. Schuster et al., APPROACHES TO THE GENETICS OF CARDIOVASCULAR-DISEASE THROUGH GENETIC FIELD WORK, Kidney international, 53(6), 1998, pp. 1449-1454
CONNEXIN-26 R143W MUTATION ASSOCIATED WITH RECESSIVE NONSYNDROMIC SENSORINEURAL DEAFNESS IN AFRICA
Authors: BROBBY GW MULLERMYHSOK B HORSTMANN RD
Citation: Gw. Brobby et al., CONNEXIN-26 R143W MUTATION ASSOCIATED WITH RECESSIVE NONSYNDROMIC SENSORINEURAL DEAFNESS IN AFRICA, The New England journal of medicine, 338(8), 1998, pp. 548-550
ROBUSTNESS AND POWER OF THE MAXIMUM-LIKELIHOOD-BINOMIAL AND MAXIMUM-LIKELIHOOD-SCOPE METHODS, IN MULTIPOINT LINKAGE ANALYSIS OF AFFECTED-SIBSHIP DATA
Authors: ABEL L MULLERMYHSOK B
Citation: L. Abel et B. Mullermyhsok, ROBUSTNESS AND POWER OF THE MAXIMUM-LIKELIHOOD-BINOMIAL AND MAXIMUM-LIKELIHOOD-SCOPE METHODS, IN MULTIPOINT LINKAGE ANALYSIS OF AFFECTED-SIBSHIP DATA, American journal of human genetics, 63(2), 1998, pp. 638-647
MAXIMUM-LIKELIHOOD EXPRESSION OF THE TRANSMISSION DISEQUILIBRIUM TESTAND POWER CONSIDERATIONS/
Authors: ABEL L MULLERMYHSOK B
Citation: L. Abel et B. Mullermyhsok, MAXIMUM-LIKELIHOOD EXPRESSION OF THE TRANSMISSION DISEQUILIBRIUM TESTAND POWER CONSIDERATIONS/, American journal of human genetics, 63(2), 1998, pp. 664-667
EVIDENCE FOR LINKAGE OF SPELLING DISABILITY TO CHROMOSOME-15
Authors: SCHULTEKORNE G GRIMM T NOTHEN MM MULLERMYHSOK B CICHON S VOGT IR PROPPING P REMSCHMIDT H
Citation: G. Schultekorne et al., EVIDENCE FOR LINKAGE OF SPELLING DISABILITY TO CHROMOSOME-15, American journal of human genetics, 63(1), 1998, pp. 279-282
LINKAGE ANALYSES OF EYE TRACKING DYSFUNCTION IN FAMILIES WITH MULTIPLE CASES OF SCHIZOPHRENIA TO CHROMOSOME 6P, 8P, AND 22Q
Authors: LENCER R AROTT V PURMANN S SCHURMANN M MULLERMYHSOK B NOLTE A KRECKER K SCHWINGER E
Citation: R. Lencer et al., LINKAGE ANALYSES OF EYE TRACKING DYSFUNCTION IN FAMILIES WITH MULTIPLE CASES OF SCHIZOPHRENIA TO CHROMOSOME 6P, 8P, AND 22Q, American journal of medical genetics, 74(6), 1997, pp. 595-595
EVIDENCE FOR LINKAGE OF SPELLING DISABILITY TO CHROMOSOME-15
Authors: SCHULTEKORNE G GRIMM T NOTHEN MM MULLERMYHSOK B PROPPING P REMSCHMIDT H
Citation: G. Schultekorne et al., EVIDENCE FOR LINKAGE OF SPELLING DISABILITY TO CHROMOSOME-15, American journal of medical genetics, 74(6), 1997, pp. 661-661
LINKAGE ANALYSES OF EYE-TRACKING DYSFUNCTION IN FAMILIES WITH MULTIPLE CASES OF SCHIZOPHRENIA TO CHROMOSOME 6P, 8P, AND 22Q
Authors: LENCER R AROLT V PURMANN S SCHURMANN M MULLERMYHSOK B NOLTE A KRECKER K SCHWINGER E
Citation: R. Lencer et al., LINKAGE ANALYSES OF EYE-TRACKING DYSFUNCTION IN FAMILIES WITH MULTIPLE CASES OF SCHIZOPHRENIA TO CHROMOSOME 6P, 8P, AND 22Q, American journal of medical genetics, 74(6), 1997, pp. 666-666
GENETIC COMPLEXITY AND PARKINSONS-DISEASE
Authors: GASSER T MULLERMYHSOK B WSZOLEK ZK DURR A VAUGHAN JR BONIFATI V MECO G BEREZNAI B OEHLMANN R AGID Y BRICE A WOOD N
Citation: T. Gasser et al., GENETIC COMPLEXITY AND PARKINSONS-DISEASE, Science, 277(5324), 1997, pp. 388-389
GENETIC-ANALYSIS OF COMPLEX DISEASES
Authors: MULLERMYHSOK B ABEL L
Citation: B. Mullermyhsok et L. Abel, GENETIC-ANALYSIS OF COMPLEX DISEASES, Science, 275(5304), 1997, pp. 1328-1329
DE-NOVO REARRANGEMENTS FOUND IN 2-PERCENT OF INDEX PATIENTS WITH SPINAL MUSCULAR-ATROPHY - MUTATIONAL MECHANISMS, PARENTAL ORIGIN, MUTATION-RATE, AND IMPLICATIONS FOR GENETIC-COUNSELING
Authors: WIRTH B SCHMIDT T HAHNEN E RUDNIKSCHONEBORN S KRAWCZAK M MULLERMYHSOK B SCHONLING J ZERRES K
Citation: B. Wirth et al., DE-NOVO REARRANGEMENTS FOUND IN 2-PERCENT OF INDEX PATIENTS WITH SPINAL MUSCULAR-ATROPHY - MUTATIONAL MECHANISMS, PARENTAL ORIGIN, MUTATION-RATE, AND IMPLICATIONS FOR GENETIC-COUNSELING, American journal of human genetics, 61(5), 1997, pp. 1102-1111
DE-NOVO REARRANGEMENTS FOUND IN 2-PERCENT INDEX PATIENTS WITH SPINAL MUSCULAR-ATROPHY - MUTATIONAL MECHANISMS, PARENTAL ORIGIN, MUTATION-RATE AND IMPLICATIONS FOR GENETIC-COUNSELING
Authors: WIRTH B SCHMIDT T HAHNEN E RUDNIKSCHONEBORN S KRAWCZAK M MULLERMYHSOK B SCHONLING J ZERRES K
Citation: B. Wirth et al., DE-NOVO REARRANGEMENTS FOUND IN 2-PERCENT INDEX PATIENTS WITH SPINAL MUSCULAR-ATROPHY - MUTATIONAL MECHANISMS, PARENTAL ORIGIN, MUTATION-RATE AND IMPLICATIONS FOR GENETIC-COUNSELING, American journal of human genetics, 61(4), 1997, pp. 2057-2057
FURTHER EVIDENCE SUGGESTING THE PRESENCE OF A LOCUS, ON HUMAN-CHROMOSOME 5Q31-Q33, INFLUENCING THE INTENSITY OF INFECTION WITH SCHISTOSOMA-MANSONI
Authors: MULLERMYHSOK B STELMA FF GUISSESOW F MUNTAU B THYE T BURCHARD GD GRYSEELS B HORSTMANN RD
Citation: B. Mullermyhsok et al., FURTHER EVIDENCE SUGGESTING THE PRESENCE OF A LOCUS, ON HUMAN-CHROMOSOME 5Q31-Q33, INFLUENCING THE INTENSITY OF INFECTION WITH SCHISTOSOMA-MANSONI, American journal of human genetics, 61(2), 1997, pp. 452-454
MAPPING UNDETECTED MUTATIONS WITHIN A GENE - EVIDENCE FOR 2 PREFERENTIAL REGIONS IN THE DMD GENE
Authors: MULLERMYHSOK B HEILAND HJ MULLER CR MENG G GRIMM T OTT J
Citation: B. Mullermyhsok et al., MAPPING UNDETECTED MUTATIONS WITHIN A GENE - EVIDENCE FOR 2 PREFERENTIAL REGIONS IN THE DMD GENE, Human heredity, 47(2), 1997, pp. 61-65
AUTOSOMAL RECESSIVE NON-SYNDROMIC DEAFNESS LOCUS (DFNB8) MAPS ON CHROMOSOME 21Q22 IN A LARGE CONSANGUINEOUS KINDRED FROM PAKISTAN
Authors: VESKE A OEHLMANN R YOUNUS F MOHYUDDIN A MULLERMYHSOK B MEHDI SQ GAL A
Citation: A. Veske et al., AUTOSOMAL RECESSIVE NON-SYNDROMIC DEAFNESS LOCUS (DFNB8) MAPS ON CHROMOSOME 21Q22 IN A LARGE CONSANGUINEOUS KINDRED FROM PAKISTAN, Human molecular genetics, 5(1), 1996, pp. 165-168
IDENTIFICATION OF A KEY RECOMBINANT NARROWS THE CADASIL GENE REGION TO 8 CM AND ARGUES AGAINST ALLELISM OF CADASIL AND FAMILIAL HEMIPLEGIC MIGRAINE
Authors: DICHGANS M MAYER M MULLERMYHSOK B STRAUBE A GASSER T
Citation: M. Dichgans et al., IDENTIFICATION OF A KEY RECOMBINANT NARROWS THE CADASIL GENE REGION TO 8 CM AND ARGUES AGAINST ALLELISM OF CADASIL AND FAMILIAL HEMIPLEGIC MIGRAINE, Genomics, 32(1), 1996, pp. 151-154
EYE TRACKING DYSFUNCTION IS A PUTATIVE PHENOTYPIC SUSCEPTIBILITY MARKER OF SCHIZOPHRENIA AND MAPS TO A LOCUS ON CHROMOSOME 6P IN FAMILIES WITH MULTIPLE OCCURRENCE OF THE DISEASE
Authors: AROLT V LENCER R NOLTE A MULLERMYHSOK B PURMANN S SCHURMANN M LEUTELT J PINNOW M SCHWINGER E
Citation: V. Arolt et al., EYE TRACKING DYSFUNCTION IS A PUTATIVE PHENOTYPIC SUSCEPTIBILITY MARKER OF SCHIZOPHRENIA AND MAPS TO A LOCUS ON CHROMOSOME 6P IN FAMILIES WITH MULTIPLE OCCURRENCE OF THE DISEASE, American journal of medical genetics, 67(6), 1996, pp. 564-579
THE CYP2D6B ALLELE IS NOT OVERREPRESENTED IN A POPULATION OF GERMAN PATIENTS WITH IDIOPATHIC PARKINSONS-DISEASE
Authors: GASSER T MULLERMYHSOK B SUPALA A ZIMMER E WIEDITZ G WSZOLEK ZK VIEREGGE P BONIFATI V OERTEL WH
Citation: T. Gasser et al., THE CYP2D6B ALLELE IS NOT OVERREPRESENTED IN A POPULATION OF GERMAN PATIENTS WITH IDIOPATHIC PARKINSONS-DISEASE, Journal of Neurology, Neurosurgery and Psychiatry, 61(5), 1996, pp. 518-520
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