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Results: 1-25 | 26-50 | 51-75 | 76-84
Results: 26-50/84
THE PRESENCE OF GENETIC ANTICIPATION SUGGESTS THAT THE MOLECULAR-BASIS OF FAMILIAL PRIMARY PULMONARY-HYPERTENSION MAY BE TRINUCLEOTIDE REPEAT EXPANSION
Authors: LOYD JE SLOVIS B PHILLIPS JA BUTLER MG FOROUD TM CONNEALLY PM NEWMAN JH
Citation: Je. Loyd et al., THE PRESENCE OF GENETIC ANTICIPATION SUGGESTS THAT THE MOLECULAR-BASIS OF FAMILIAL PRIMARY PULMONARY-HYPERTENSION MAY BE TRINUCLEOTIDE REPEAT EXPANSION, Chest, 111(6), 1997, pp. 82-83
PHOTOANTHROPOMETRIC STUDY OF CRANIOFACIAL TRAITS IN INDIVIDUALS WITH WILLIAMS-SYNDROME
Authors: HOVIS CL BUTLER MG
Citation: Cl. Hovis et Mg. Butler, PHOTOANTHROPOMETRIC STUDY OF CRANIOFACIAL TRAITS IN INDIVIDUALS WITH WILLIAMS-SYNDROME, Clinical genetics, 51(6), 1997, pp. 379-387
PILOT-STUDIES FOR PROFICIENCY TESTING USING FLUORESCENCE IN-SITU HYBRIDIZATION WITH CHROMOSOME-SPECIFIC DNA PROBES - A COLLEGE-OF-AMERICAN-PATHOLOGISTS AMERICAN-COLLEGE-OF-MEDICAL-GENETICS PROGRAM
Authors: DEWALD GW BROTHMAN AR BUTLER MG COOLEY LD PATIL SR SAIKEVYCH IA SCHNEIDER NR
Citation: Gw. Dewald et al., PILOT-STUDIES FOR PROFICIENCY TESTING USING FLUORESCENCE IN-SITU HYBRIDIZATION WITH CHROMOSOME-SPECIFIC DNA PROBES - A COLLEGE-OF-AMERICAN-PATHOLOGISTS AMERICAN-COLLEGE-OF-MEDICAL-GENETICS PROGRAM, Archives of pathology and laboratory medicine, 121(4), 1997, pp. 359-367
COMPARISON OF CHROMOSOME TELOMERE INTEGRITY IN MULTIPLE TISSUES FROM INDIVIDUALS AT DIFFERENT AGES
Authors: TILBURT J DEVRIES A AUE G SCHWARTZ HS BETHI M ATKINSON J HEDGES LK BUTLER MG
Citation: J. Tilburt et al., COMPARISON OF CHROMOSOME TELOMERE INTEGRITY IN MULTIPLE TISSUES FROM INDIVIDUALS AT DIFFERENT AGES, American journal of human genetics, 61(4), 1997, pp. 941-941
GENETIC-VARIANTS OF THE HUMAN OBESITY (OB) GENE IN PRADER-WILLI-SYNDROME AND CONTROL INDIVIDUALS - COMPARISON WITH BODY-MASS INDEX AND WEIGHT
Authors: BUTLER MG HEDGES LK HOVIS CL FEURER I
Citation: Mg. Butler et al., GENETIC-VARIANTS OF THE HUMAN OBESITY (OB) GENE IN PRADER-WILLI-SYNDROME AND CONTROL INDIVIDUALS - COMPARISON WITH BODY-MASS INDEX AND WEIGHT, American journal of human genetics, 61(4), 1997, pp. 1781-1781
TELOMERASE ACTIVITY IN SKELETAL SARCOMAS
Authors: AUE G BETHI M SCHWARTZ HS BUTLER MG
Citation: G. Aue et al., TELOMERASE ACTIVITY IN SKELETAL SARCOMAS, American journal of human genetics, 61(4), 1997, pp. 2110-2110
MICROSATELLITE INSTABILITY IN MALIGNANT-MELANOMA OF SOFT PARTS
Authors: SCHWARTZ HS AUE G BUTLER MG
Citation: Hs. Schwartz et al., MICROSATELLITE INSTABILITY IN MALIGNANT-MELANOMA OF SOFT PARTS, American journal of human genetics, 61(4), 1997, pp. 2134-2134
BREAKAGE IN THE SNRPN LOCUS IN A BALANCED 46,XY,T(15-19) PRADER-WILLI-SYNDROME PATIENT
Authors: SUN YM NICHOLLS RD BUTLER MG SAITOH S HAINLINE BE PALMER CG
Citation: Ym. Sun et al., BREAKAGE IN THE SNRPN LOCUS IN A BALANCED 46,XY,T(15-19) PRADER-WILLI-SYNDROME PATIENT, Human molecular genetics, 5(4), 1996, pp. 517-524
MRI OF POSTERIOR KNEE MASSES
Authors: BUTLER MG FUCHIGAMI KD CHAKO A
Citation: Mg. Butler et al., MRI OF POSTERIOR KNEE MASSES, Skeletal radiology, 25(4), 1996, pp. 309-317
FAMILIAL DOUBLE PERICENTRIC-INVERSION OF CHROMOSOME-5 WITH SOME FEATURES OF CRI-DU-CHAT SYNDROME
Authors: GOODART SA BUTLER MG OVERHAUSER J
Citation: Sa. Goodart et al., FAMILIAL DOUBLE PERICENTRIC-INVERSION OF CHROMOSOME-5 WITH SOME FEATURES OF CRI-DU-CHAT SYNDROME, Human genetics, 97(6), 1996, pp. 802-807
LACK OF MICROSATELLITE INSTABILITY IN GIANT-CELL TUMOR OF BONE
Authors: SCHEINER M HEDGES L SCHWARTZ HS BUTLER MG
Citation: M. Scheiner et al., LACK OF MICROSATELLITE INSTABILITY IN GIANT-CELL TUMOR OF BONE, Cancer genetics and cytogenetics, 88(1), 1996, pp. 35-38
CHROMOSOME TELOMERE INTEGRITY OF HUMAN SOLID NEOPLASMS
Authors: BUTLER MG SCIADINI M HEDGES LK SCHWARTZ HS
Citation: Mg. Butler et al., CHROMOSOME TELOMERE INTEGRITY OF HUMAN SOLID NEOPLASMS, Cancer genetics and cytogenetics, 86(1), 1996, pp. 50-53
BRIEF CLINICAL REPORT - A 5-YEAR-OLD WHITE GIRL WITH PRADER-WILLI-SYNDROME AND A SUBMICROSCOPIC DELETION OF CHROMOSOME-15Q11Q13
Authors: BUTLER MG CHRISTIAN SL KUBOTA T LEDBETTER DH
Citation: Mg. Butler et al., BRIEF CLINICAL REPORT - A 5-YEAR-OLD WHITE GIRL WITH PRADER-WILLI-SYNDROME AND A SUBMICROSCOPIC DELETION OF CHROMOSOME-15Q11Q13, American journal of medical genetics, 65(2), 1996, pp. 137-141
AN OVERVIEW OF THE VANDERBILT-UNIVERSITY PRADER-WILLI-SYNDROME PROGRAM PROJECT
Authors: THOMPSON T BUTLER MG
Citation: T. Thompson et Mg. Butler, AN OVERVIEW OF THE VANDERBILT-UNIVERSITY PRADER-WILLI-SYNDROME PROGRAM PROJECT, American journal of medical genetics, 64(4), 1996, pp. 17-17
COINHERITANCE OF OTHER CHROMOSOME-15 ABNORMALITIES WITH PRADER-WILLI-SYNDROME - GENETIC RISK-ESTIMATION AND MAPPING
Authors: ROGAN PK MASCARI MJ LADDA RL WOODAGE T TRENT RJ SMITH A LAI LW ERICKSON RP CASSIDY SB PETERSEN MB MIKKELSEN M DRISCOLL DJ NICHOLLS RD BUTLER MG
Citation: Pk. Rogan et al., COINHERITANCE OF OTHER CHROMOSOME-15 ABNORMALITIES WITH PRADER-WILLI-SYNDROME - GENETIC RISK-ESTIMATION AND MAPPING, American journal of medical genetics, 62(3), 1996, pp. 6-6
MOLECULAR CYTOGENETIC ANALYSIS OF A PRADER-WILLI-SYNDROME PATIENT WITH A DE-NOVO 46,XY, T(15-19)(Q12-Q13.41)
Authors: SUN Y BUTLER MG HAINLINE BE PALMER CG
Citation: Y. Sun et al., MOLECULAR CYTOGENETIC ANALYSIS OF A PRADER-WILLI-SYNDROME PATIENT WITH A DE-NOVO 46,XY, T(15-19)(Q12-Q13.41), American journal of medical genetics, 62(3), 1996, pp. 8-8
DISTINCT 15Q GENOTYPES IN RUSSELL-SILVER AND RING-15 SYNDROMES
Authors: ROGAN PK SEIP JR DRISCOLL DJ PAPENHAUSEN PR JOHNSON VP RASKIN S WOODWARD AL BUTLER MG
Citation: Pk. Rogan et al., DISTINCT 15Q GENOTYPES IN RUSSELL-SILVER AND RING-15 SYNDROMES, American journal of medical genetics, 62(1), 1996, pp. 10-15
MOLECULAR DIAGNOSIS OF PRADER-WILLI-SYNDROME - COMPARISON OF CYTOGENETIC AND MOLECULAR-GENETIC DATA INCLUDING PARENT OF ORIGIN DEPENDENT METHYLATION DNA PATTERNS
Authors: BUTLER MG
Citation: Mg. Butler, MOLECULAR DIAGNOSIS OF PRADER-WILLI-SYNDROME - COMPARISON OF CYTOGENETIC AND MOLECULAR-GENETIC DATA INCLUDING PARENT OF ORIGIN DEPENDENT METHYLATION DNA PATTERNS, American journal of medical genetics, 61(2), 1996, pp. 188-190
RADIOLOGIC ASSESSMENT OF BODY-COMPOSITION IN PATIENTS WITH PRADER-WILLI-SYNDROME
Authors: RIDDLE WR PRICE RR BUTLER MG EWING S
Citation: Wr. Riddle et al., RADIOLOGIC ASSESSMENT OF BODY-COMPOSITION IN PATIENTS WITH PRADER-WILLI-SYNDROME, Radiology, 201, 1996, pp. 822-822
SHOULD THE 3C (CRANIOCEREBELLOCARDIAC) SYNDROME BE INCLUDED IN THE SPECTRUM OF VELOCARDIOFACIAL SYNDROME AND DIGEORGE SEQUENCE
Authors: BUTLER MG MOWREY P
Citation: Mg. Butler et P. Mowrey, SHOULD THE 3C (CRANIOCEREBELLOCARDIAC) SYNDROME BE INCLUDED IN THE SPECTRUM OF VELOCARDIOFACIAL SYNDROME AND DIGEORGE SEQUENCE, Journal of Medical Genetics, 33(8), 1996, pp. 719-720
CYTOGENETIC DIFFERENTIATION OF NATURAL AN D LABORATORY POPULATIONS OFCAMPTOCHIRONOMUS TENTANS (FABRICIUS) (CHIRONOMIDAE, DIPTERA)
Authors: GUNDERINA LI KIKNADZE II AIMANOVA KG ISTOMINA AG PROVIZ VI SALOVA TA RAKISHEVA AZ BUTLER MG
Citation: Li. Gunderina et al., CYTOGENETIC DIFFERENTIATION OF NATURAL AN D LABORATORY POPULATIONS OFCAMPTOCHIRONOMUS TENTANS (FABRICIUS) (CHIRONOMIDAE, DIPTERA), Genetika, 32(1), 1996, pp. 53-67
GEOGRAPHIC-VARIATION IN THE POLYTENE CHROMOSOME-BANDING PATTERN OF THE HOLARCTIC MIDGE CHIRONOMUS (CAMPTOCHIRONOMUS) TENTANS (FABRICIUS)
Authors: KIKNADZE II BUTLER MG AIMANOVA KG GUNDERINA LI COOPER JK
Citation: Ii. Kiknadze et al., GEOGRAPHIC-VARIATION IN THE POLYTENE CHROMOSOME-BANDING PATTERN OF THE HOLARCTIC MIDGE CHIRONOMUS (CAMPTOCHIRONOMUS) TENTANS (FABRICIUS), Canadian journal of zoology, 74(1), 1996, pp. 171-191
DIAGNOSTIC TESTING FOR PRADER-WILLI AND ANGELMAN SYNDROMES - REPORT OF THE ASHC ACMC TEST AND TECHNOLOGY-TRANSFER COMMITTEE/
Authors: CASSIDY SB BEAUDET AL KNOLL JHM LEDBETTER DH NICHOLLS RD SCHWARTZ S BUTLER MG WATSON M
Citation: Sb. Cassidy et al., DIAGNOSTIC TESTING FOR PRADER-WILLI AND ANGELMAN SYNDROMES - REPORT OF THE ASHC ACMC TEST AND TECHNOLOGY-TRANSFER COMMITTEE/, American journal of human genetics, 58(5), 1996, pp. 1085-1088
GENETIC ANTICIPATION AND ABNORMAL GENDER RATIO AT BIRTH IN FAMILIAL PRIMARY PULMONARY-HYPERTENSION
Authors: LOYD JE BUTLER MG FOROUD TM CONNEALLY PM PHILLIPS JA NEWMAN JH
Citation: Je. Loyd et al., GENETIC ANTICIPATION AND ABNORMAL GENDER RATIO AT BIRTH IN FAMILIAL PRIMARY PULMONARY-HYPERTENSION, American journal of respiratory and critical care medicine, 152(1), 1995, pp. 93-97
USE OF FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) IN THE DIAGNOSIS OF DIGEORGE SEQUENCE AND RELATED DISEASES
Authors: LARSON RS BUTLER MG
Citation: Rs. Larson et Mg. Butler, USE OF FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) IN THE DIAGNOSIS OF DIGEORGE SEQUENCE AND RELATED DISEASES, Diagnostic molecular pathology, 4(4), 1995, pp. 274-278
Risultati: 1-25 | 26-50 | 51-75 | 76-84