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Results: 1-7 |
Results: 7
MULTILOCUS LINKAGE IDENTIFIES 2 NEW LOCI FOR A MENDELIAN FORM OF STROKE, CEREBRAL CAVERNOUS MALFORMATION, AT 7P15-13 AND 3Q25.2-27
Authors: CRAIG HD GUNEL M CEPEDA O JOHNSON EW PTACEK L STEINBERG GK OGILVY CS BERG MJ CRAWFORD SC SCOTT RM STEICHENGERSDORF E SABROE R KENNEDY CTC METTLER G BEIS MJ FRYER A AWAD IA LIFTON RP
Citation: Hd. Craig et al., MULTILOCUS LINKAGE IDENTIFIES 2 NEW LOCI FOR A MENDELIAN FORM OF STROKE, CEREBRAL CAVERNOUS MALFORMATION, AT 7P15-13 AND 3Q25.2-27, Human molecular genetics (Print), 7(12), 1998, pp. 1851-1858
CHARACTERIZATION OF X-17(Q12-P13) TRANSLOCATION BREAKPOINTS IN A FEMALE-PATIENT WITH HYPOMELANOSIS OF ITO AND CHOROID-PLEXUS PAPILLOMA
Authors: ZAJAC V KIRCHHOFF T LEVY ER HORSLEY SW MILLER A STEICHENGERSDORF E MONACO AP
Citation: V. Zajac et al., CHARACTERIZATION OF X-17(Q12-P13) TRANSLOCATION BREAKPOINTS IN A FEMALE-PATIENT WITH HYPOMELANOSIS OF ITO AND CHOROID-PLEXUS PAPILLOMA, European journal of human genetics, 5(2), 1997, pp. 61-68
PERSISTENT HYPERPLASTIC PRIMARY VITREOUS IN A FAMILY WITH OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME
Authors: STEICHENGERSDORF E GASSNER I UNSINN K SPERL W
Citation: E. Steichengersdorf et al., PERSISTENT HYPERPLASTIC PRIMARY VITREOUS IN A FAMILY WITH OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME, Clinical dysmorphology, 6(2), 1997, pp. 171-176
DELETION MAPPING ON CHROMOSOME 17P IN MEDULLOBLASTOMA
Authors: STEICHENGERSDORF E BAUMGARTNER M KRECZY A MAIER H FINK FM
Citation: E. Steichengersdorf et al., DELETION MAPPING ON CHROMOSOME 17P IN MEDULLOBLASTOMA, British Journal of Cancer, 76(10), 1997, pp. 1284-1287
LOCALIZATION OF THE BREAST-OVARIAN CANCER SUSCEPTIBILITY GENE (BRCAI)ON 17Q12-21 TO AN INTERVAL OF LESS-THAN-OR-EQUAL-TO-ICM
Authors: SMITH SA DICIOCCIO RA STRUEWING JP EASTON DF GALLION HH ALBERTSEN H MAZOYER S JOHANSSON B STEICHENGERSDORF E STRATTON M FORD D MARSHALL G WHITE RL PIVER MS PONDER BAJ
Citation: Sa. Smith et al., LOCALIZATION OF THE BREAST-OVARIAN CANCER SUSCEPTIBILITY GENE (BRCAI)ON 17Q12-21 TO AN INTERVAL OF LESS-THAN-OR-EQUAL-TO-ICM, Genes, chromosomes & cancer, 10(1), 1994, pp. 71-76
A FAMILY WITH VISCERAL COURSE OF NIEMANN-PICK DISEASE, MACULAR HALO SYNDROME AND LOW SPHINGOMYELIN DEGRADATION RATE
Authors: SPERL W BART G VANIER MT CHRISTOMANOU H BALDISSERA I STEICHENGERSDORF E PASCHKE E
Citation: W. Sperl et al., A FAMILY WITH VISCERAL COURSE OF NIEMANN-PICK DISEASE, MACULAR HALO SYNDROME AND LOW SPHINGOMYELIN DEGRADATION RATE, Journal of inherited metabolic disease, 17(1), 1994, pp. 93-103
FAMILIAL SITE-SPECIFIC OVARIAN-CANCER IS LINKED TO BRCA1 ON 17Q12-21
Authors: STEICHENGERSDORF E GALLION HH FORD D GIRODET C EASTON DF DICIOCCIO RA EVANS G PONDER MA PYE C MAZOYER S NOGUCHI T KARENGUEVEN F SOBOL H HARDOUIN A BIGNON YJ PIVER MS SMITH SA PONDER BAJ
Citation: E. Steichengersdorf et al., FAMILIAL SITE-SPECIFIC OVARIAN-CANCER IS LINKED TO BRCA1 ON 17Q12-21, American journal of human genetics, 55(5), 1994, pp. 870-875
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