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Results:
1-15
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Results: 15
Authors:
KORF B
Citation: B. Korf, PITFALLS IN THE INTERPRETATION OF MOLECULAR DIAGNOSTIC TESTS. (VOL 10, PG 368, 1996), Journal of clinical laboratory analysis, 12(1), 1998, pp. 75-75
Authors:
PRASAD C
QUACKENBUSH EJ
WHITEMAN D
KORF B
Citation: C. Prasad et al., LIMB ANOMALIES IN DIGEORGE AND CHARGE SYNDROMES, American journal of medical genetics, 68(2), 1997, pp. 179-181
Authors:
GUTMANN DH
AYLSWORTH A
CAREY JC
KORF B
MARKS J
PYERITZ RE
RUBENSTEIN A
VISKOCHIL D
Citation: Dh. Gutmann et al., THE DIAGNOSTIC EVALUATION AND MULTIDISCIPLINARY MANAGEMENT OF NEUROFIBROMATOSIS-1 AND NEUROFIBROMATOSIS-2, JAMA, the journal of the American Medical Association, 278(1), 1997, pp. 51-57
Authors:
KNOLL KHM
REPETTO G
DERKALOUSTIAN V
MUNDLOS C
EYDOUX P
KORF B
WHITE LM
Citation: Khm. Knoll et al., LARGE DICENTRIC CHROMOSOME 15Q11Q13 DUPLICATIONS - MULTIPLE REGIONS OF BREAKAGE, MECHANISMS OF FORMATION AND CLINICAL FINDINGS, American journal of human genetics, 61(4), 1997, pp. 23-23
Authors:
BASSON CT
MACRAE CA
KORF B
MERLISS A
Citation: Ct. Basson et al., GENETIC-HETEROGENEITY OF FAMILIAL ATRIAL-MYXOMA SYNDROMES (CARNEY COMPLEX), The American journal of cardiology, 79(7), 1997, pp. 994
ALLELE-SPECIFIC REPLICATION OF 15Q11-Q13 LOCI - A DIAGNOSTIC-TEST FORDETECTION OF UNIPARENTAL DISOMY
Authors:
WHITE LM
ROGAN PK
NICHOLLS RD
WU BL
KORF B
KNOLL JHM
Citation: Lm. White et al., ALLELE-SPECIFIC REPLICATION OF 15Q11-Q13 LOCI - A DIAGNOSTIC-TEST FORDETECTION OF UNIPARENTAL DISOMY, American journal of human genetics, 59(2), 1996, pp. 423-430
Authors:
ESTABROOKS LL
RAO KW
DRISCOLL DA
CRANDALL BF
DEAN JCS
IKONEN E
KORF B
AYLSWORTH AS
Citation: Ll. Estabrooks et al., PRELIMINARY PHENOTYPIC MAP OF CHROMOSOME 4P16 BASED ON 4P DELETIONS, American journal of medical genetics, 57(4), 1995, pp. 581-586
Authors:
NEEDLE MN
MOLLOY PT
PACKER R
FRIEDMAN HS
COHEN BH
JAKACKI R
KORF B
VAUGHAN SN
PHILLIPS PC
Citation: Mn. Needle et al., A PHASE-II RANDOMIZED TRIAL OF 13-CIS RETINOIC ACID (CRA) AND INTERFERON ALFA-2A (IFN) IN THE TREATMENT OF PLEXIFORM NEUROFIBROMA (PN) IN PATIENTS WITH NEUROFIBROMATOSIS TYPE-1 (NF1), Pediatric research, 37(4), 1995, pp. 151-151
Authors:
KORF B
Citation: B. Korf, MOLECULAR MEDICINE - MOLECULAR DIAGNOSIS .2. (VOL 332, PG 1499, 1995), The New England journal of medicine, 333(5), 1995, pp. 331-331
Authors:
KORF B
Citation: B. Korf, MOLECULAR MEDICINE - MOLECULAR DIAGNOSIS .2., The New England journal of medicine, 332(22), 1995, pp. 1499-1502
Authors:
KORF B
Citation: B. Korf, MOLECULAR DIAGNOSIS .1., The New England journal of medicine, 332(18), 1995, pp. 1218-1220
ALLELE-SPECIFIC REPLICATION OF 15Q11Q13 LOCI - A DIAGNOSTIC-TEST FOR DETECTION OF UNIPARENTAL DISOMY
Authors:
KNOLL JHM
ROGAN PK
NICHOLLS RD
WU B
KORF B
WHITE L
Citation: Jhm. Knoll et al., ALLELE-SPECIFIC REPLICATION OF 15Q11Q13 LOCI - A DIAGNOSTIC-TEST FOR DETECTION OF UNIPARENTAL DISOMY, American journal of human genetics, 57(4), 1995, pp. 165-165
Authors:
ZIMMER C
KORF B
EBEL H
TRAUPE H
Citation: C. Zimmer et al., CENTRAL NEUROCYTOMA - DIFFERENTIAL-DIAGNO SIS OF INTRAVENTRICULAR TUMORS, Aktuelle Neurologie, 20(4), 1993, pp. 132-137
Authors:
SATLER C
WALSH E
KORF B
GINSBURG G
KUNKEL L
NADALGINARD B
Citation: C. Satler et al., CLEAR EVIDENCE FOR GENETIC-HETEROGENEITY AMONG LARGE MULTIGENERATIONAL FAMILIES WITH LONG QT SYNDROME, Circulation, 88(4), 1993, pp. 573-573
Authors:
ESTABROOKS LL
RAO KW
DRISCOLL DA
IKONEN E
KORF B
CRANDALL BF
AYLSWORTH AS
Citation: Ll. Estabrooks et al., A PRELIMINARY PHENOTYPIC MAP OF CHROMOSOME-4P16, American journal of human genetics, 53(3), 1993, pp. 1288-1288
Risultati:
1-15
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