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Results: 1-25 | 26-50 | 51-59
Results: 26-50/59
LOCALIZATION OF CAV1, A CANDIDATE GENE FOR NEURAL-TUBE DEFECTS, TO 7Q31
Authors: VILES KD GILBERT J STRITTMATTER W GEORGE TM SPEER MC
Citation: Kd. Viles et al., LOCALIZATION OF CAV1, A CANDIDATE GENE FOR NEURAL-TUBE DEFECTS, TO 7Q31, American journal of human genetics, 61(4), 1997, pp. 2301-2301
LINKAGE OF FAMILIAL DILATED CARDIOMYOPATHY WITH CONDUCTION DEFECT ANDMUSCULAR-DYSTROPHY TO CHROMOSOME 6Q23
Authors: MESSINA DN SPEER MC PERICAKVANCE MA MCNALLY EM
Citation: Dn. Messina et al., LINKAGE OF FAMILIAL DILATED CARDIOMYOPATHY WITH CONDUCTION DEFECT ANDMUSCULAR-DYSTROPHY TO CHROMOSOME 6Q23, American journal of human genetics, 61(4), 1997, pp. 909-917
TYPE-VI COLLAGEN MUTATIONS IN BETHLEM MYOPATHY, AN AUTOSOMAL-DOMINANTMYOPATHY WITH CONTRACTURES
Authors: JOBSIS GJ KEIZERS H VREIJLING JP DEVISSER M SPEER MC WOLTERMAN RA BAAS F BOLHUIS PA
Citation: Gj. Jobsis et al., TYPE-VI COLLAGEN MUTATIONS IN BETHLEM MYOPATHY, AN AUTOSOMAL-DOMINANTMYOPATHY WITH CONTRACTURES, Nature genetics, 14(1), 1996, pp. 113-115
EVIDENCE FOR LOCUS HETEROGENEITY IN THE BETHLEM MYOPATHY AND LINKAGE TO 2Q37
Authors: SPEER MC TANDAN R RAO PN FRIES T STAJICH JM BOLHUIS PA JOBSIS GJ VANCE JM VILES KD SHEFFIELD K JAMES C KAHLER SG PETTENATI M GILBERT JR DENTON PH YAMAOKA LH PERICAKVANCE MA
Citation: Mc. Speer et al., EVIDENCE FOR LOCUS HETEROGENEITY IN THE BETHLEM MYOPATHY AND LINKAGE TO 2Q37, Human molecular genetics, 5(7), 1996, pp. 1043-1046
GENETIC-STUDIES OF COMPLEX DISEASES - LET THE READER BEWARE
Authors: ECONS MJ SPEER MC
Citation: Mj. Econs et Mc. Speer, GENETIC-STUDIES OF COMPLEX DISEASES - LET THE READER BEWARE, Journal of bone and mineral research, 11(12), 1996, pp. 1835-1840
MISCLASSIFICATION AND LINKAGE OF HEREDITARY SENSORY AND AUTONOMIC NEUROPATHY TYPE-1 AS CHARCOT-MARIE-TOOTH DISEASE, TYPE 2B
Authors: VANCE JM SPEER MC STAJICH JM WEST S WOLPERT C GASKELL P LENNON F TIM RM ROZEAR M BENOTHMANE K
Citation: Jm. Vance et al., MISCLASSIFICATION AND LINKAGE OF HEREDITARY SENSORY AND AUTONOMIC NEUROPATHY TYPE-1 AS CHARCOT-MARIE-TOOTH DISEASE, TYPE 2B, American journal of human genetics, 59(1), 1996, pp. 258-260
DATA SIMULATION FOR GAW9 PROBLEMS 1 AND 2
Authors: SPEER MC TERWILLIGER JD OTT J
Citation: Mc. Speer et al., DATA SIMULATION FOR GAW9 PROBLEMS 1 AND 2, Genetic epidemiology, 12(6), 1995, pp. 561-564
CONFIRMATION OF LOCUS HETEROGENEITY IN THE PURE FORM OF FAMILIAL SPASTIC PARAPLEGIA
Authors: SPEER MC KINGSTON HM BOUSTANY RMN GASKELL PC ROBINSON LC LENNON F WOLPERT CM YAMAOKA LH KAHLER SG HOGAN EL CUMMING WJK PERICAKVANCE MA
Citation: Mc. Speer et al., CONFIRMATION OF LOCUS HETEROGENEITY IN THE PURE FORM OF FAMILIAL SPASTIC PARAPLEGIA, American journal of medical genetics, 60(4), 1995, pp. 307-311
BETHLEM MYOPATHY IS NOT ALLELIC TO LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 1A
Authors: SPEER MC YAMAOKA LH STAJICH J LEWIS K PERICAKVANCE MA STACY R TANDAN R FRIES TJ
Citation: Mc. Speer et al., BETHLEM MYOPATHY IS NOT ALLELIC TO LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 1A, American journal of medical genetics, 58(2), 1995, pp. 197-198
EXCLUSION MAPPING OF CHROMOSOMAL REGIONS WHICH CROSS HYBRIDIZE TO FSHD1A ASSOCIATED MARKERS IN FSHD1B
Authors: GILBERT JR SPEER MC STAJICH J CLANCY R LEWIS K QIU H YAMAOKA L KUMAR A VANCE J STEWART C ROZEAR M ROSES AD PERICAKVANCE MA
Citation: Jr. Gilbert et al., EXCLUSION MAPPING OF CHROMOSOMAL REGIONS WHICH CROSS HYBRIDIZE TO FSHD1A ASSOCIATED MARKERS IN FSHD1B, Journal of Medical Genetics, 32(10), 1995, pp. 770-773
EVIDENCE FOR LOCUS HETEROGENEITY IN AUTOSOMAL-DOMINANT LIMB-GIRDLE MUSCULAR-DYSTROPHY
Authors: SPEER MC GILCHRIST JM CHUTKOW JG MCMICHAEL R WESTBROOK CA STAJICH JM JORGENSON EM GASKELL PC ROSI BL RAMESAR R VANCE JM YAMAOKA LH ROSES AD PERICAKVANCE MA
Citation: Mc. Speer et al., EVIDENCE FOR LOCUS HETEROGENEITY IN AUTOSOMAL-DOMINANT LIMB-GIRDLE MUSCULAR-DYSTROPHY, American journal of human genetics, 57(6), 1995, pp. 1371-1376
THE UTILITY OF INTRAOCULAR-PRESSURE AS A QUANTITATIVE TRAIT FOR GENETIC-LINKAGE ANALYSIS
Authors: ALLINGHAM RR DAMII KF SPEER MC PRITCHARD M HAINES JL PERICAKVANCE MA
Citation: Rr. Allingham et al., THE UTILITY OF INTRAOCULAR-PRESSURE AS A QUANTITATIVE TRAIT FOR GENETIC-LINKAGE ANALYSIS, American journal of human genetics, 57(4), 1995, pp. 441-441
LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2C (LGMD2C) - IDENTIFICATION OF LINKAGE DISEQUILIBRIUM AND INITIATION OF A PHYSICAL MAP SPANNING THE REGION
Authors: BENOTHMANE K DENTON P SPEER MC STAUFFER J LOEB D RAO N MIDDLETON ML BENHAMIDA M PERICAKVANCE MA VANCE JM
Citation: K. Benothmane et al., LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2C (LGMD2C) - IDENTIFICATION OF LINKAGE DISEQUILIBRIUM AND INITIATION OF A PHYSICAL MAP SPANNING THE REGION, American journal of human genetics, 57(4), 1995, pp. 1071-1071
PEDIGENE - A COMPREHENSIVE DATA MANAGEMENT-SYSTEM TO FACILITATE EFFICIENT AND RAPID DISEASE GENE-MAPPING
Authors: HAYNES C SPEER MC PEEDIN M ROSES AD HAINES JL VANCE JM PERICAKVANCE MA
Citation: C. Haynes et al., PEDIGENE - A COMPREHENSIVE DATA MANAGEMENT-SYSTEM TO FACILITATE EFFICIENT AND RAPID DISEASE GENE-MAPPING, American journal of human genetics, 57(4), 1995, pp. 1106-1106
LOCUS HETEROGENEITY AND LINKAGE TO 2Q IN THE BETHLEM MYOPATHY
Authors: SPEER MC TANDAN R STAJICH JM VILES KD SHEFFIELD K JAMES C BOLHUIS P VANCE JM FRIES T YAMAOKA LH PERICAKVANCE MA
Citation: Mc. Speer et al., LOCUS HETEROGENEITY AND LINKAGE TO 2Q IN THE BETHLEM MYOPATHY, American journal of human genetics, 57(4), 1995, pp. 1323-1323
EXCLUSION MAPPING OF CHROMOSOMAL REGIONS WHICH CROSS-HYBRIDIZE TO FSH1A ASSOCIATED MARKERS IN FSH1B
Authors: YAMAOKA L SPEER MC STAJICH J LEWIS K CLANCY R QIU H KUMAR A VANCE J STEWART C ROZEAR M ROSES AD PERICALVANCE MA GILBERT JR
Citation: L. Yamaoka et al., EXCLUSION MAPPING OF CHROMOSOMAL REGIONS WHICH CROSS-HYBRIDIZE TO FSH1A ASSOCIATED MARKERS IN FSH1B, American journal of human genetics, 57(4), 1995, pp. 1905-1905
EVIDENCE FOR LINKAGE DISEQUILIBRIUM IN CHROMOSOME 13-LINKED DUCHENNE-LIKE MUSCULAR-DYSTROPHY (LGMD2C)
Authors: BENOTHMANE K SPEER MC STAUFFER J BLEL S MIDDLETON L BENHAMIDA C ETRIBI A LOEB D HENTATI F ROSES AD BENHAMIDA M PERICAKVANCE MA VANCE JM
Citation: K. Benothmane et al., EVIDENCE FOR LINKAGE DISEQUILIBRIUM IN CHROMOSOME 13-LINKED DUCHENNE-LIKE MUSCULAR-DYSTROPHY (LGMD2C), American journal of human genetics, 57(3), 1995, pp. 732-734
LINKAGE OF RECESSIVE FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS TO CHROMOSOME 2Q33-Q35
Authors: HENTATI A BEJAOUI K PERICAKVANCE MA HENTATI F SPEER MC HUNG WY FIGLEWICZ DA HAINES J RIMMLER J BENHAMIDA C BENHAMIDA M BROWN RH SIDDIQUE T
Citation: A. Hentati et al., LINKAGE OF RECESSIVE FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS TO CHROMOSOME 2Q33-Q35, Nature genetics, 7(3), 1994, pp. 425-428
DINUCLEOTIDE REPEAT POLYMORPHISM AT THE DXS1683 LOCUS
Authors: ECONS MJ FRANCIS F ROWE PSN SPEER MC ORIORDAN JLH LEHRACH H BECKER PA
Citation: Mj. Econs et al., DINUCLEOTIDE REPEAT POLYMORPHISM AT THE DXS1683 LOCUS, Human molecular genetics, 3(4), 1994, pp. 680-680
DEVELOPMENT OF A MICROSATELLITE GENETIC-MAP SPANNING 5Q31-Q33 AND SUBSEQUENT PLACEMENT OF THE LGMD1A LOCUS BETWEEN D5S178 AND IL9
Authors: YAMAOKA LH WESTBROOK CA SPEER MC GILCHRIST JM JABS EW SCHWEINS EG STAJICH JM GASKELL PC ROSES AD PERICAKVANCE MA
Citation: Lh. Yamaoka et al., DEVELOPMENT OF A MICROSATELLITE GENETIC-MAP SPANNING 5Q31-Q33 AND SUBSEQUENT PLACEMENT OF THE LGMD1A LOCUS BETWEEN D5S178 AND IL9, Neuromuscular disorders, 4(5-6), 1994, pp. 471-475
PHYSICAL AND GENETIC-MAP OF 5Q31 - USE OF FLUORESCENCE IN-SITU HYBRIDIZATION DATA TO IDENTIFY ERRORS IN THE CEPH DATABASE
Authors: WESTBROOK CA LEBEAU MM NEUMAN WL KEINANEN M YAMAOKA LH SPEER MC ESPINOSA R NAKAMURA Y WILLIAMSON R MULLAN M BUETOW K
Citation: Ca. Westbrook et al., PHYSICAL AND GENETIC-MAP OF 5Q31 - USE OF FLUORESCENCE IN-SITU HYBRIDIZATION DATA TO IDENTIFY ERRORS IN THE CEPH DATABASE, Cytogenetics and cell genetics, 67(2), 1994, pp. 86-93
LINKAGE ANALYSIS OF A CANDIDATE LOCUS (HLA) IN AUTOSOMAL-DOMINANT SACRAL DEFECT WITH ANTERIOR MENINGOCELE
Authors: CHATKUPT S SPEER MC DING YL THOMAS M STENROOS ES DERMODY JJ KOENIGSBERGER MR OTT J JOHNSON WG
Citation: S. Chatkupt et al., LINKAGE ANALYSIS OF A CANDIDATE LOCUS (HLA) IN AUTOSOMAL-DOMINANT SACRAL DEFECT WITH ANTERIOR MENINGOCELE, American journal of medical genetics, 52(1), 1994, pp. 1-4
RISK OF INTRACRANIAL ANEURYSMS IN FAMILIES WITH SUBARACHNOID HEMORRHAGE
Authors: ALBERTS MJ SPEER MC QUINONES A GRAFFAGNINO C FRIEDMAN A ROSES AD
Citation: Mj. Alberts et al., RISK OF INTRACRANIAL ANEURYSMS IN FAMILIES WITH SUBARACHNOID HEMORRHAGE, Stroke, 25(1), 1994, pp. 248-248
FINE-STRUCTURE MAPPING OF THE HUMAN X-LINKED HYPOPHOSPHATEMIC RICKETSGENE LOCUS
Authors: ECONS MJ ROWE PSN FRANCIS F BARKER DF SPEER MC NORMAN M PAIN PR WEISSENBACH J READ A DAVIS KE BECKER PA LEHRACH H ORIORDAN J DREZNER MK
Citation: Mj. Econs et al., FINE-STRUCTURE MAPPING OF THE HUMAN X-LINKED HYPOPHOSPHATEMIC RICKETSGENE LOCUS, The Journal of clinical endocrinology and metabolism, 79(5), 1994, pp. 1351-1354
GENETIC AND PHYSICAL MAPPING OF THE TREACHER-COLLINS SYNDROME LOCUS WITH RESPECT TO LOCI IN THE CHROMOSOME-5Q3 REGION
Authors: JABS EW LI X LOVETT M YAMAOKA LH TAYLOR E SPEER MC COSS C CADLE R HALL B BROWN K KIDD KK DOLGANOV G POLYMEROPOULOS MH MEYERS DA
Citation: Ew. Jabs et al., GENETIC AND PHYSICAL MAPPING OF THE TREACHER-COLLINS SYNDROME LOCUS WITH RESPECT TO LOCI IN THE CHROMOSOME-5Q3 REGION, Genomics, 18(1), 1993, pp. 7-13
Risultati: 1-25 | 26-50 | 51-59