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Results: 1-11 |
Results: 11
MALIGNANT NERVOUS-SYSTEM TUMORS IN NEUROFIBROMATOSIS-2
Authors: BASER ME MACCOLLIN MM EVANS DGR ALLEN J JACKLER RK SUJANSKY E RUBENSTEIN AE LOUIS DN
Citation: Me. Baser et al., MALIGNANT NERVOUS-SYSTEM TUMORS IN NEUROFIBROMATOSIS-2, American journal of human genetics, 61(4), 1997, pp. 321-321
NEUROFIBROMATOSIS TYPE-1 AND PREGNANCY
Authors: DUGOFF L SUJANSKY E
Citation: L. Dugoff et E. Sujansky, NEUROFIBROMATOSIS TYPE-1 AND PREGNANCY, American journal of medical genetics, 66(1), 1996, pp. 7-10
STURGE-WEBER SYNDROME - AGE-OF-ONSET OF SEIZURES AND GLAUCOMA AND THEPROGNOSIS FOR AFFECTED CHILDREN
Authors: SUJANSKY E CONRADI S
Citation: E. Sujansky et S. Conradi, STURGE-WEBER SYNDROME - AGE-OF-ONSET OF SEIZURES AND GLAUCOMA AND THEPROGNOSIS FOR AFFECTED CHILDREN, Journal of child neurology, 10(1), 1995, pp. 49-58
OUTCOME OF STURGE-WEBER SYNDROME IN 52 ADULTS
Authors: SUJANSKY E CONRADI S
Citation: E. Sujansky et S. Conradi, OUTCOME OF STURGE-WEBER SYNDROME IN 52 ADULTS, American journal of medical genetics, 57(1), 1995, pp. 35-45
COMPARATIVE GENOMIC HYBRIDIZATION (CGH) IDENTIFIES PARTIAL MONOSOMIESAND TRISOMIES IN PATIENTS WITH UNBALANCED KARYOTYPES
Authors: MCGAVRAN L MELTESEN L BURNETT M SUJANSKY E MCKENZIE P LUNT B PARKER NB MANCHESTER DK
Citation: L. Mcgavran et al., COMPARATIVE GENOMIC HYBRIDIZATION (CGH) IDENTIFIES PARTIAL MONOSOMIESAND TRISOMIES IN PATIENTS WITH UNBALANCED KARYOTYPES, American journal of human genetics, 57(4), 1995, pp. 81-81
PLEXIFORM NEUROFIBROMAS IN NEUROFIBROMATOSIS TYPE-1 (NF1) - THE OUTCOME OF SURGERY
Authors: SUJANSKY E CONRADI S
Citation: E. Sujansky et S. Conradi, PLEXIFORM NEUROFIBROMAS IN NEUROFIBROMATOSIS TYPE-1 (NF1) - THE OUTCOME OF SURGERY, American journal of human genetics, 57(4), 1995, pp. 278-278
RECOMBINANT-8 SYNDROME BREAKPOINT ANALYSIS
Authors: PATTERSON D SUJANSKY E HART I BLESKAN J WALTON K GIANG J SHECTER I
Citation: D. Patterson et al., RECOMBINANT-8 SYNDROME BREAKPOINT ANALYSIS, American journal of human genetics, 57(4), 1995, pp. 501-501
BONE DYSPLASIAS OF INFANCY IN THE VIENNA COLLECTION
Authors: BEIGHTON P SUJANSKY E PATZAK B PORTELE KA
Citation: P. Beighton et al., BONE DYSPLASIAS OF INFANCY IN THE VIENNA COLLECTION, Pediatric radiology, 24(6), 1994, pp. 384-386
MOLECULAR-GENETIC TESTING OF A FETUS AT RISK OF GERSTMANN-STRAUSSLER-SCHEINKER SYNDROME
Authors: BROWN P CERVENAKOVA L GOLDFARB LG GAJDUSEK DC HAVERKAMP A HAVERKAMP C HORWITZ J CREACY SD BEVER RA WEXLER P SUJANSKY E BJORK RJ
Citation: P. Brown et al., MOLECULAR-GENETIC TESTING OF A FETUS AT RISK OF GERSTMANN-STRAUSSLER-SCHEINKER SYNDROME, Lancet, 343(8890), 1994, pp. 181-182
GENETIC SKELETAL DYSPLASIAS IN THE MUSEUM OF PATHOLOGICAL ANATOMY, VIENNA
Authors: BEIGHTON P SUJANSKY E PATZAK B PORTELE KA
Citation: P. Beighton et al., GENETIC SKELETAL DYSPLASIAS IN THE MUSEUM OF PATHOLOGICAL ANATOMY, VIENNA, American journal of medical genetics, 47(6), 1993, pp. 843-847
NATURAL-HISTORY OF THE RECOMBINANT-(8) SYNDROME
Authors: SUJANSKY E SMITH ACM PRESCOTT KE FREEHAUF CL CLERICUZIO C ROBINSON A
Citation: E. Sujansky et al., NATURAL-HISTORY OF THE RECOMBINANT-(8) SYNDROME, American journal of medical genetics, 47(4), 1993, pp. 512-525
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