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Results: 6

Authors: KADAKOL A DEOCHARAN B MUKHOPADHYAY L CHOWDHURY JR CHOWDHURY NR
Citation: A. Kadakol et al., RAPID PRENATAL-DIAGNOSIS OF CRIGLER-NAJJAR SYNDROME TYPE-1 BY GENETIC-ANALYSIS OF CHORIONIC VILLUS SAMPLES, Hepatology, 28(4), 1998, pp. 615-615

Authors: GANTLA S BAKKER CTM DEOCHARAN B THUMMALA NR ZWEINER J SINAASAPPEL M CHOWDHURY JR BOSMA PJ CHOWDHURY NR
Citation: S. Gantla et al., SPLICE-SITE MUTATIONS - A NOVEL GENETIC MECHANISM OF CRIGLER-NAJJAR SYNDROME TYPE-1, American journal of human genetics, 62(3), 1998, pp. 585-592

Authors: CHOWDHURY NR DEOCHARAN B BEJJANKI HR GANTLA S CHOUDHURY JR KOLIOPOULOS C PETMEZAKI S VALAES T
Citation: Nr. Chowdhury et al., THE PRESENCE OF A GILBERT-TYPE PROMOTER ABNORMALITY INCREASES THE LEVEL OF NEONATAL HYPERBILILRUBINEMIA, Hepatology, 26(4), 1997, pp. 967-967

Authors: DEOCHARAN B GANTLA S MORTON DH RIZACK L CHOWDHURY JR CHOWDHURY NR
Citation: B. Deocharan et al., INTERACTION OF A CRIGLER-NAJJAR-SYNDROME TYPE-I MUTATION AND A GILBERT-TYPE PROMOTER DEFECT RESULTS IN 2 GRADES OF HYPERBILIRUBINEMIA IN MEMBERS OF AN AMISH AND A MENNONITE KINDRED OF LANCASTER COUNTY, PENNSYLVANIA, Gastroenterology, 112(4), 1997, pp. 1255-1255

Authors: GANTLA S DEOCHARAN B SENGUPTA K THUMMALA NR ZWEINER J BOSMA PJ CHOWDHURY JR CHOWDHURY NR
Citation: S. Gantla et al., INTRONIC MUTATION - A NOVEL GENETIC MECHANISM OF CRIGLER-NAJJAR SYNDROME TYPE-I, Hepatology, 24(4), 1996, pp. 496-496

Authors: KIM BH CHOWDHURY NR DEOCHARAN B JAUREGUI H SCHUMACHER IK FOX IJ CHOWDHURY JR
Citation: Bh. Kim et al., AMELIORATION OF BILIRUBIN CONJUGATION DEFECT IN GUNN-RATS BY TRANSPLANTING CONDITIONALLY IMMORTALIZED HEPATOCYTES, Hepatology, 22(4), 1995, pp. 417-417
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