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Results: 1-6 |
Results: 6

Authors: CRNIC I LEVANAT S SITUM M BASTAJUZBASIC A PAVELIC K
Citation: I. Crnic et al., MOLECULAR-GENETIC ANALYSIS OF NBCCS REGION IN PATIENTS WITH BASOCELLULAR CARCINOMA AND NBCCS, European journal of human genetics, 6, 1998, pp. 4275-4275

Authors: LEVANAT S CHIDAMBARAM A WICKING C BRAYWARD P PRESSMAN C TOFTGARD R GAILANI MR MYERS JC WAINWRIGHT B DEAN M BALE AE
Citation: S. Levanat et al., PULSED-FIELD GEL-ELECTROPHORESIS AND FISH MAPPING OF CHROMOSOME 9Q22 - PLACEMENT OF A NOVEL ZINC-FINGER GENE WITHIN THE NBCCS AND ESS1 REGION, Cytogenetics and cell genetics, 76(3-4), 1997, pp. 208-213

Authors: LEVANAT S GORLIN RJ FALLET S JOHNSON DR FANTASIA JE BALE AE
Citation: S. Levanat et al., A 2-HIT MODEL FOR DEVELOPMENTAL DEFECTS IN GORLIN-SYNDROME, Nature genetics, 12(1), 1996, pp. 85-87

Authors: SHIMKETS R GAILANI MR SIU VM YANGFENG T PRESSMAN CL LEVANAT S GOLDSTEIN A DEAN M BALE AE
Citation: R. Shimkets et al., MOLECULAR ANALYSIS OF CHROMOSOME 9Q DELETIONS IN 2 GORLIN SYNDROME PATIENTS, American journal of human genetics, 59(2), 1996, pp. 417-422

Authors: JOHNSON DR LEVANAT S BALE AE
Citation: Dr. Johnson et al., DIRECT MOLECULAR ANALYSIS OF ARCHIVAL TUMOR-TISSUE FOR LOSS OF HETEROZYGOSITY, BioTechniques, 19(2), 1995, pp. 190

Authors: BALE AE GORLIN RJ FALLET S JOHNSON DR LEVANAT S
Citation: Ae. Bale et al., A 2-HIT MODEL FOR DEVELOPMENTAL DEFECTS IN GORLIN-SYNDROME, American journal of human genetics, 57(4), 1995, pp. 62-62
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