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Results: 1-25 | 26-38
Results: 1-25/38
PERMANENT COMMITTEE OF THE INTERNATIONAL CONGRESSES OF HUMAN-GENETICS
Authors: MULVIHILL JJ BERG K
Citation: Jj. Mulvihill et K. Berg, PERMANENT COMMITTEE OF THE INTERNATIONAL CONGRESSES OF HUMAN-GENETICS, American journal of medical genetics, 79(2), 1998, pp. 79-81
FAMILIAL EOSINOPHILIA - CLINICAL AND LABORATORY RESULTS ON A US KINDRED
Authors: LIN AY NUTMAN TB KASLOW D MULVIHILL JJ FONTAINE L WHITE BJ KNUTSEN T THEIL KS RAGHUPRASAD PK GOLDSTEIN AM TUCKER MA
Citation: Ay. Lin et al., FAMILIAL EOSINOPHILIA - CLINICAL AND LABORATORY RESULTS ON A US KINDRED, American journal of medical genetics, 76(3), 1998, pp. 229-237
ENCOMIUM - MILLER,ROBERT,WARWICK - MENTOR, SYNTHESIZER, AND INTERNATIONAL INTERDISCIPLINARY INITIATOR
Authors: MULVIHILL JJ
Citation: Jj. Mulvihill, ENCOMIUM - MILLER,ROBERT,WARWICK - MENTOR, SYNTHESIZER, AND INTERNATIONAL INTERDISCIPLINARY INITIATOR, American journal of medical genetics, 76(1), 1998, pp. 1-8
SURGICAL-MANAGEMENT OF SPINAL-CORD COMPRESSION FROM PLEXIFORM NEUROFIBROMAS IN PATIENTS WITH NEUROFIBROMATOSIS-1
Authors: POLLACK IF COLAK A FITZ C WIENER E MORELAND M MULVIHILL JJ
Citation: If. Pollack et al., SURGICAL-MANAGEMENT OF SPINAL-CORD COMPRESSION FROM PLEXIFORM NEUROFIBROMAS IN PATIENTS WITH NEUROFIBROMATOSIS-1, Neurosurgery, 43(2), 1998, pp. 248-255
GENETIC-DISEASE IN OFFSPRING OF LONG-TERM SURVIVORS OF CHILDHOOD AND ADOLESCENT CANCER
Authors: BYRNE J RASMUSSEN SA STEINHORN SC CONNELLY RR MYERS MH LYNCH CF FLANNERY J AUSTIN DF HOLMES FF HOLMES GE STRONG LC MULVIHILL JJ
Citation: J. Byrne et al., GENETIC-DISEASE IN OFFSPRING OF LONG-TERM SURVIVORS OF CHILDHOOD AND ADOLESCENT CANCER, American journal of human genetics, 62(1), 1998, pp. 45-52
NEUROFIBROMATOSIS-1 AND NEUROFIBROMATOSIS-2
Authors: POLLACK IF MULVIHILL JJ
Citation: If. Pollack et Jj. Mulvihill, NEUROFIBROMATOSIS-1 AND NEUROFIBROMATOSIS-2, Brain pathology, 7(2), 1997, pp. 823-836
SPECTRUM OF MALIGNANCY AND PREMALIGNANCY IN CARNEY-SYNDROME
Authors: NWOKORO NA KORYTKOWSKI MT ROSE S GORIN MB STADLER MP WITCHEL SF MULVIHILL JJ
Citation: Na. Nwokoro et al., SPECTRUM OF MALIGNANCY AND PREMALIGNANCY IN CARNEY-SYNDROME, American journal of medical genetics, 73(4), 1997, pp. 369-377
INTERSTITIAL LUNG-DISEASE IN AN ADULT WITH FANCONI-ANEMIA - CLUES TO THE PATHOGENESIS
Authors: RUBINSTEIN WS WENGER SL HOFFMAN RM AUERBACH AD MULVIHILL JJ
Citation: Ws. Rubinstein et al., INTERSTITIAL LUNG-DISEASE IN AN ADULT WITH FANCONI-ANEMIA - CLUES TO THE PATHOGENESIS, American journal of medical genetics, 69(3), 1997, pp. 315-319
CHOLESTEROL AND BILE-ACID REPLACEMENT THERAPY IN CHILDREN AND ADULTS WITH SMITH-LEMLI-OPITZ (SLO RSH) SYNDROME/
Authors: NWOKORO NA MULVIHILL JJ
Citation: Na. Nwokoro et Jj. Mulvihill, CHOLESTEROL AND BILE-ACID REPLACEMENT THERAPY IN CHILDREN AND ADULTS WITH SMITH-LEMLI-OPITZ (SLO RSH) SYNDROME/, American journal of medical genetics, 68(3), 1997, pp. 315-321
FAMILIAL PHEOCHROMOCYTOMA DUE TO MUTANT VON-HIPPEL-LINDAU-DISEASE GENE
Authors: MULVIHILL JJ FERRELL RE CARTY SE TISHERMAN SE ZBAR B
Citation: Jj. Mulvihill et al., FAMILIAL PHEOCHROMOCYTOMA DUE TO MUTANT VON-HIPPEL-LINDAU-DISEASE GENE, Archives of internal medicine, 157(12), 1997, pp. 1390-1391
SEGREGATION ANALYSIS OF PANCREATIC-CANCER
Authors: ASTON CE BANKE MG MCNAMARA PJ CROWLEY KE MULVIHILL JJ
Citation: Ce. Aston et al., SEGREGATION ANALYSIS OF PANCREATIC-CANCER, American journal of human genetics, 61(4), 1997, pp. 1117-1117
FAMILIAL AGGREGATION OF OTHER CANCERS IN FAMILIES WITH PANCREATIC-CANCER
Authors: CROWLEY KE ASTON CE MACNAMARA PJ MULVIHILL JJ
Citation: Ke. Crowley et al., FAMILIAL AGGREGATION OF OTHER CANCERS IN FAMILIES WITH PANCREATIC-CANCER, American journal of human genetics, 61(4), 1997, pp. 1134-1134
A UNIQUE POINT MUTATION IN THE FIBROBLAST-GROWTH-FACTOR-RECEPTOR-3 GENE (FGFR3) DEFINES A NEW CRANIOSYNOSTOSIS SYNDROME
Authors: MUENKE M GRIPP KW MCDONALDMCGINN DM GAUDENZ K WHITAKER LA BARTLETT SP MARKOWITZ RI ROBIN NH NWOKORO N MULVIHILL JJ LOSKEN HW MULLIKEN JB GUTTMACHER AE WILROY RS CLARKE LA HOLLWAY G ADES LC HAAN EA MULLEY JC COHEN MM BELLUS GA FRANCOMANO CA MOLONEY DM WALL SA WILKIE AOM ZACKAI EH
Citation: M. Muenke et al., A UNIQUE POINT MUTATION IN THE FIBROBLAST-GROWTH-FACTOR-RECEPTOR-3 GENE (FGFR3) DEFINES A NEW CRANIOSYNOSTOSIS SYNDROME, American journal of human genetics, 60(3), 1997, pp. 555-564
LOCALIZATION OF THE GENE FOR COWDEN DISEASE TO CHROMOSOME 10Q22-23
Authors: NELEN MR PADBERG GW PEETERS EAJ LIN AY VANDENHELM B FRANTS RR COULON V GOLDSTEIN AM VANREEN MMM EASTON DF EELES RA HODGSON S MULVIHILL JJ MURDAY VA TUCKER MA MARIMAN ECM STARINK TM PONDER BAJ ROPERS HH KREMER H LONGY M ENG C
Citation: Mr. Nelen et al., LOCALIZATION OF THE GENE FOR COWDEN DISEASE TO CHROMOSOME 10Q22-23, Nature genetics, 13(1), 1996, pp. 114-116
GERMLINE MUTATIONS IN THE VON-HIPPEL-LINDAU DISEASE (VHL) GENE IN FAMILIES FROM NORTH-AMERICA, EUROPE, AND JAPAN
Authors: ZBAR B KISHIDA T CHEN F SCHMIDT L MAHER ER RICHARDS FM CROSSEY PA WEBSTER AR AFFARA NA FERGUSONSMITH MA BRAUCH H GLAVAC D NEUMANN HPH TISHERMAN S MULVIHILL JJ GROSS DJ SHUIN T WHALEY J SEIZINGER B KLEY N OLSCHWANG S BOISSON C RICHARD S LIPS CHM LINEHAN WM LERMAN M
Citation: B. Zbar et al., GERMLINE MUTATIONS IN THE VON-HIPPEL-LINDAU DISEASE (VHL) GENE IN FAMILIES FROM NORTH-AMERICA, EUROPE, AND JAPAN, Human mutation, 8(4), 1996, pp. 348-357
INTERNATIONAL GENETIC WORKSHOP ON CROUZON-DISEASE AND OTHER CRANIOFACIAL DISORDERS, PITTSBURGH, PA, MARCH 10-11, 1995
Authors: POST JC MULVIHILL JJ EHRLICH GD
Citation: Jc. Post et al., INTERNATIONAL GENETIC WORKSHOP ON CROUZON-DISEASE AND OTHER CRANIOFACIAL DISORDERS, PITTSBURGH, PA, MARCH 10-11, 1995, Archives of otolaryngology, head & neck surgery, 122(5), 1996, pp. 576-578
GRAPHS TO ESTIMATE AN INDIVIDUALIZED RISK OF BREAST-CANCER
Authors: BENICHOU J GAIL MH MULVIHILL JJ
Citation: J. Benichou et al., GRAPHS TO ESTIMATE AN INDIVIDUALIZED RISK OF BREAST-CANCER, Journal of clinical oncology, 14(1), 1996, pp. 103-110
SPECIAL ISSUES IN THE MANAGEMENT OF GLIOMAS IN CHILDREN WITH NEUROFIBROMATOSIS-1
Authors: POLLACK IF MULVIHILL JJ
Citation: If. Pollack et Jj. Mulvihill, SPECIAL ISSUES IN THE MANAGEMENT OF GLIOMAS IN CHILDREN WITH NEUROFIBROMATOSIS-1, Journal of neuro-oncology, 28(2-3), 1996, pp. 257-268
THE FLOATING-HARBOR-SYNDROME WITH CARDIAC SEPTAL-DEFECT
Authors: LAZEBNIK N MCPHERSON E RITTMEYER LJ MULVIHILL JJ
Citation: N. Lazebnik et al., THE FLOATING-HARBOR-SYNDROME WITH CARDIAC SEPTAL-DEFECT, American journal of medical genetics, 66(3), 1996, pp. 300-302
THE MANAGEMENT OF BRAIN-STEM GLIOMAS IN PATIENTS WITH NEUROFIBROMATOSIS-1
Authors: POLLACK IF SHULTZ B MULVIHILL JJ
Citation: If. Pollack et al., THE MANAGEMENT OF BRAIN-STEM GLIOMAS IN PATIENTS WITH NEUROFIBROMATOSIS-1, Neurology, 46(6), 1996, pp. 1652-1660
BREAST-CANCER RISK ANALYSIS AND COUNSELING
Authors: MULVIHILL JJ STADLER MP
Citation: Jj. Mulvihill et Mp. Stadler, BREAST-CANCER RISK ANALYSIS AND COUNSELING, Clinical obstetrics and gynecology, 39(4), 1996, pp. 851-859
LYMPHANGIOSARCOMA IN LATE-ONSET HEREDITARY LYMPHEDEMA - CASE-REPORT AND NOSOLOGICAL IMPLICATIONS
Authors: ANDERSSON HC PARRY DM MULVIHILL JJ
Citation: Hc. Andersson et al., LYMPHANGIOSARCOMA IN LATE-ONSET HEREDITARY LYMPHEDEMA - CASE-REPORT AND NOSOLOGICAL IMPLICATIONS, American journal of medical genetics, 56(1), 1995, pp. 72-75
10Q26 - CONSISTENT CHROMOSOMAL BREAKPOINT IN 2 CARDIAC MYXOMAS FROM APATIENT WITH CARNEY-SYNDROME
Authors: GOLLIN SM JENKINS RB SWANEY WP MULVIHILL JJ BARTELT D NWOKORO NA
Citation: Sm. Gollin et al., 10Q26 - CONSISTENT CHROMOSOMAL BREAKPOINT IN 2 CARDIAC MYXOMAS FROM APATIENT WITH CARNEY-SYNDROME, American journal of human genetics, 57(4), 1995, pp. 343-343
INADVERTENT OFF-PROTOCOL TESTING FOR COLON CANCER-PREDISPOSING GENE HMSH2
Authors: MULVIHILL JJ ELLIS CE STADLER MP LUCE MC
Citation: Jj. Mulvihill et al., INADVERTENT OFF-PROTOCOL TESTING FOR COLON CANCER-PREDISPOSING GENE HMSH2, American journal of human genetics, 57(4), 1995, pp. 388-388
CONCORDANCE OF CLINICAL FINDINGS IN SIBLINGS WITH THE SMITH-LEMLI-OPITZ SYNDROME
Authors: CUNNIFF CM ABUELO DN ARN PH BARNSHAD MJ CAREY JC NWOKORO NA MULVIHILL JJ ZACKAI EH KELLEY RI
Citation: Cm. Cunniff et al., CONCORDANCE OF CLINICAL FINDINGS IN SIBLINGS WITH THE SMITH-LEMLI-OPITZ SYNDROME, American journal of human genetics, 57(4), 1995, pp. 471-471
Risultati: 1-25 | 26-38