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1P36 : every subband a suppressor
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Balanced translocation in a neuroblastoma patient disrupts a cluster of small nuclear RNA UI and tRNA genes in chromosomal band Ip36
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Deletion mapping in neuroblastoma cell-lines suggests 2 distinct tumor-suppressor genes in the lp35-36 region, only one of which is associated with N-myc amplification.
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Characterization of the chromosome breakpoints in a patient with a constitutional translocation T(1-17)(P36.31-P36.13-Q11.2-Q12) and neuroblastoma.
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Assignment of the human beta-catenin gene (CTNNB1) to 3p22->p21.3 by fluorescence in situ hybridization.
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Blepharophimosis-ptosis-epicanthus inversus syndrome (BPES): clinical subtypes and their genotype
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Full triploidy in a liveborn preterm infant.
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Identification of 2 distinct chromosome-12-derived amplification units in neuroblastoma cell-line NGP.
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THE GENE FOR HUMAN GAP JUNCTION PROTEIN CONNEXIN37 (GJA4) MAPS TO CHROMOSOME 1P35.1, IN THE VICINITY OF D1S195.
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CONSTITUTIONAL TRANSLOCATION T(1-17)(P36.31-P36.13-Q11.2Q12.1) IN A NEUROBLASTOMA PATIENT. ESTABLISHMENT OF SOMATIC-CELL HYBRIDS AND IDENTIFICATION OF PND/A12M2 ON CHROMOSOME-1 AND NF1/SCYA7 ON CHROMOSOME-17 AS BREAKPOINT FLANKING SINGLE-COPY MARKERS.