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Results: 1-6 |
Results: 6

Authors: CROOP JM TILLER GE FLETCHER JA LUX ML RAAB E GOLDENSON D SON D ARCINIEGAS S WU RL
Citation: Jm. Croop et al., ISOLATION AND CHARACTERIZATION OF A MAMMALIAN HOMOLOG OF THE DROSOPHILA WHITE GENE, Gene, 185(1), 1997, pp. 77-85

Authors: XIAO S LUX ML REEVES R HUDSON TJ FLETCHER JA
Citation: S. Xiao et al., HMGI(Y) ACTIVATION BY CHROMOSOME 6P21 REARRANGEMENTS IN MULTILINEAGE MESENCHYMAL CELLS FROM PULMONARY HAMARTOMA, The American journal of pathology, 150(3), 1997, pp. 901-910

Authors: EBER SW GONZALEZ JM LUX ML SCARPA AL TSE WT DORNWELL M HERBERS J KUGLER W OZCAN R PEKRUN A GALLAGHER PG SCHROTER W FORGET BG LUX SE
Citation: Sw. Eber et al., ANKYRIN-1 MUTATIONS ARE A MAJOR CAUSE OF DOMINANT AND RECESSIVE HEREDITARY SPHEROCYTOSIS, Nature genetics, 13(2), 1996, pp. 214-218

Authors: NAEEM R LUX ML HUANG SF NABER SP CORSON JM FLETCHER JA
Citation: R. Naeem et al., RING CHROMOSOMES IN DERMATOFIBROSARCOMA PROTUBERANS ARE COMPOSED OF INTERSPERSED SEQUENCES FROM CHROMOSOME-17 AND CHROMOSOME-22, The American journal of pathology, 147(6), 1995, pp. 1553-1558

Authors: EBER SW GONZALEZ JM LUX ML GALLAGHER PG FORGET BG LUX SE
Citation: Sw. Eber et al., INVESTIGATIONS OF 14-ANKYRIN POLYMORPHISMS EXCLUDE LARGE DELETIONS OFTHE ANKYRIN GENE AS A MAJOR CAUSE OF HEREDITARY SPHEROCYTOSIS, Blood, 84(10), 1994, pp. 10000008-10000008

Authors: EBER SW LUX ML GONZALEZ JM SCARPA A TSE WT GALLAGHER PG PEKRUN A FORGET BG LUX SE
Citation: Sw. Eber et al., DISCOVERY OF 8 ANKYRIN MUTATIONS IN HEREDITARY SPHEROCYTOSIS (HS) INDICATES THAT ANKYRIN DEFECTS ARE A MAJOR CAUSE OF DOMINANT AND RECESSIVE HS, Blood, 82(10), 1993, pp. 10000308-10000308
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