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Results: 1-9 |
Results: 9
THE FAMILIAL WILMS-TUMOR SUSCEPTIBILITY GENE, FWT1, MAY NOT BE A TUMOR-SUPPRESSOR GENE
Authors: RAHMAN N ARBOUR L TONIN P BARUCHEL S PRITCHARDJONES K NAROD SA STRATTON MR
Citation: N. Rahman et al., THE FAMILIAL WILMS-TUMOR SUSCEPTIBILITY GENE, FWT1, MAY NOT BE A TUMOR-SUPPRESSOR GENE, Oncogene, 14(25), 1997, pp. 3099-3102
AN AUTOSOMAL-DOMINANT FORM OF FAMILIAL PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY, NOT LINKED TO THE SULFONYLUREA RECEPTOR LOCUS
Authors: KUKUVITIS A DEAL C ARBOUR L POLYCHRONAKOS C
Citation: A. Kukuvitis et al., AN AUTOSOMAL-DOMINANT FORM OF FAMILIAL PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY, NOT LINKED TO THE SULFONYLUREA RECEPTOR LOCUS, The Journal of clinical endocrinology and metabolism, 82(4), 1997, pp. 1192-1194
CHARACTERIZATION OF THE FAMILIAL WILMS-TUMOR GENE FWT1
Authors: RAHMAN N ARBOUR L TONIN P SCHWARTZ C NAROD SA PRITCHARDJONES K STRATTON MR
Citation: N. Rahman et al., CHARACTERIZATION OF THE FAMILIAL WILMS-TUMOR GENE FWT1, American journal of human genetics, 61(4), 1997, pp. 434-434
RELATION BETWEEN THE C677T POLYMORPHISM IN THE MTHFR GENE, THE FOLATELEVELS IN RED-BLOOD-CELLS, AND RISK FOR NEURAL-TUBE DEFECTS
Authors: CHRISTENSEN B ARBOUR L TRAN P SABBAGHIAN N PLATT R GILFIX B ROSENBLATT DS FORBES P ROZEN R
Citation: B. Christensen et al., RELATION BETWEEN THE C677T POLYMORPHISM IN THE MTHFR GENE, THE FOLATELEVELS IN RED-BLOOD-CELLS, AND RISK FOR NEURAL-TUBE DEFECTS, American journal of human genetics, 61(4), 1997, pp. 854-854
EVIDENCE FOR A FAMILIAL WILMS-TUMOR GENE (FWT1) ON CHROMOSOME 17Q12-Q21
Authors: RAHMAN N ARBOUR L TONIN P RENSHAW J PELLETIER J BARUCHEL S PRITCHARDJONES K STRATTON MR NAROD SA
Citation: N. Rahman et al., EVIDENCE FOR A FAMILIAL WILMS-TUMOR GENE (FWT1) ON CHROMOSOME 17Q12-Q21, Nature genetics, 13(4), 1996, pp. 461-463
GLUTATHIONE DEFICIENCY AS A COMPLICATION OF METHYLMALONIC ACIDEMIA - RESPONSE TO HIGH-DOSES OF ASCORBATE
Authors: TREACY E ARBOUR L CHESSEX P GRAHAM G KASPRZAK L CASEY K BELL L MAMER O SCRIVER CR
Citation: E. Treacy et al., GLUTATHIONE DEFICIENCY AS A COMPLICATION OF METHYLMALONIC ACIDEMIA - RESPONSE TO HIGH-DOSES OF ASCORBATE, The Journal of pediatrics, 129(3), 1996, pp. 445-448
MULTIFACTORIAL INHERITANCE OF NON-SYNDROMIC MACROCEPHALY
Authors: ARBOUR L WATTERS GV HALL JG FRASER FC
Citation: L. Arbour et al., MULTIFACTORIAL INHERITANCE OF NON-SYNDROMIC MACROCEPHALY, Clinical genetics, 50(2), 1996, pp. 57-62
INCREASED RATE OF CONGENITAL HEART-DEFECTS AMONG THE INUIT OF BAFFIN-ISLAND
Authors: GILPIN CA ARBOUR L PEKELES G PAQUET M EYDOUX P
Citation: Ca. Gilpin et al., INCREASED RATE OF CONGENITAL HEART-DEFECTS AMONG THE INUIT OF BAFFIN-ISLAND, American journal of human genetics, 57(4), 1995, pp. 495-495
IN-VITRO FERTILIZATION AND FAMILY HISTORY OF BREAST-CANCER
Authors: ARBOUR L NAROD S GLENDON G POLLAK M SEYMOUR R MINER L LEUNG P
Citation: L. Arbour et al., IN-VITRO FERTILIZATION AND FAMILY HISTORY OF BREAST-CANCER, Lancet, 344(8922), 1994, pp. 610-611
Risultati: 1-9 |