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Results: 1-8 |
Results: 8
SPERMINE DEFICIENCY IN GY MICE CAUSED BY DELETION OF THE SPERMINE SYNTHASE GENE
Authors: LORENZ B FRANCIS F GEMPEL K BODDRICH A JOSTEN M SCHMAHL W SCHMIDT J LEHRACH H MEITINGER T STROM TM
Citation: B. Lorenz et al., SPERMINE DEFICIENCY IN GY MICE CAUSED BY DELETION OF THE SPERMINE SYNTHASE GENE, Human molecular genetics, 7(3), 1998, pp. 541-547
NEW EVIDENCE FOR A MUTATION HOTSPOT IN EXON-37 OF THE NF1 GENE
Authors: BODDRICH A ROBINSON PN SCHULKE M BUSKE A TINSCHERT S NURNBERG P
Citation: A. Boddrich et al., NEW EVIDENCE FOR A MUTATION HOTSPOT IN EXON-37 OF THE NF1 GENE, Human mutation, 9(4), 1997, pp. 374-377
GENOMIC ORGANIZATION OF THE HUMAN PEX GENE MUTATED IN X-LINKED DOMINANT HYPOPHOSPHATEMIC RICKETS
Authors: FRANCIS F STROM TM HENNIG S BODDRICH A LORENZ B BRANDAU O MOHNIKE KL CAGNOLI M STEFFENS C KLAGES S BORZYM K POHL T OUDET C ECONS MJ ROWE PSN REINHARDT R MEITINGER T LEHRACH H
Citation: F. Francis et al., GENOMIC ORGANIZATION OF THE HUMAN PEX GENE MUTATED IN X-LINKED DOMINANT HYPOPHOSPHATEMIC RICKETS, PCR methods and applications, 7(6), 1997, pp. 573-585
PEX GENE DELETIONS IN GY AND HYP MICE PROVIDE MOUSE MODELS FOR X-LINKED HYPOPHOSPHATEMIA
Authors: STROM TM FRANCIS F LORENZ B BODDRICH A ECONS MJ LEHRACH H MEITINGER T
Citation: Tm. Strom et al., PEX GENE DELETIONS IN GY AND HYP MICE PROVIDE MOUSE MODELS FOR X-LINKED HYPOPHOSPHATEMIA, Human molecular genetics, 6(2), 1997, pp. 165-171
SPERMINE DEFICIENCY IN GY MICE CAUSED BY DELETION OF THE SPERMINE SYNTHASE GENE
Authors: LORENZ B FRANCIS F GEMPEL K BODDRICH A JOSTEN M SCHMAHL W GERBITZ KD LEHRACH H MEITINGER T STROM TM
Citation: B. Lorenz et al., SPERMINE DEFICIENCY IN GY MICE CAUSED BY DELETION OF THE SPERMINE SYNTHASE GENE, American journal of human genetics, 61(4), 1997, pp. 1982-1982
3 NOVEL MUTATIONS OF THE NF1 GENE DETECTED BY TEMPERATURE-GRADIENT GEL-ELECTROPHORESIS OF EXON-5 AND EXON-8
Authors: HORN D ROBINSON PN BODDRICH A BUSKE A TINSCHERT S NURNBERG P
Citation: D. Horn et al., 3 NOVEL MUTATIONS OF THE NF1 GENE DETECTED BY TEMPERATURE-GRADIENT GEL-ELECTROPHORESIS OF EXON-5 AND EXON-8, Electrophoresis, 17(10), 1996, pp. 1559-1563
2 RECURRENT NONSENSE MUTATIONS AND A 4-BP DELETION IN A QUASI-SYMMETRICAL ELEMENT IN EXON-37 OF THE NF1 GENE
Authors: ROBINSON PN BODDRICH A PETERS H TINSCHERT S BUSKE A KAUFMANN D NURNBERG P
Citation: Pn. Robinson et al., 2 RECURRENT NONSENSE MUTATIONS AND A 4-BP DELETION IN A QUASI-SYMMETRICAL ELEMENT IN EXON-37 OF THE NF1 GENE, Human genetics, 96(1), 1995, pp. 95-98
REDUCED NEUROFIBROMIN CONTENT BUT NORMAL GAP ACTIVITY IN A PATIENT WITH NEUROFIBROMATOSIS TYPE-1 CAUSED BY A 5-BASE-PAIR DUPLICATION IN EXON 12B OF THE NF1 GENE
Authors: BODDRICH A GRIESSER J HORN D KAUFMANN D KRONE W NURNBERG P
Citation: A. Boddrich et al., REDUCED NEUROFIBROMIN CONTENT BUT NORMAL GAP ACTIVITY IN A PATIENT WITH NEUROFIBROMATOSIS TYPE-1 CAUSED BY A 5-BASE-PAIR DUPLICATION IN EXON 12B OF THE NF1 GENE, Biochemical and biophysical research communications, 214(3), 1995, pp. 895-904
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