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Results: 1-16 |
Results: 16
LESS IS MORE - COMPACT GENOMES PAY DIVIDENDS
Authors: ANGRIST M
Citation: M. Angrist, LESS IS MORE - COMPACT GENOMES PAY DIVIDENDS, PCR methods and applications, 8(7), 1998, pp. 683-685
HUMAN GFRA1 - CLONING, MAPPING, GENOMIC STRUCTURE, AND EVALUATION AS A CANDIDATE GENE FOR HIRSCHSPRUNG DISEASE SUSCEPTIBILITY
Authors: ANGRIST M JING SQ BOLK S BENTLEY K NALLASAMY S HALUSHKA M FOX GM CHAKRAVARTI A
Citation: M. Angrist et al., HUMAN GFRA1 - CLONING, MAPPING, GENOMIC STRUCTURE, AND EVALUATION AS A CANDIDATE GENE FOR HIRSCHSPRUNG DISEASE SUSCEPTIBILITY, Genomics, 48(3), 1998, pp. 354-362
DOES PHASTER MEAN BETTER
Authors: ANGRIST M
Citation: M. Angrist, DOES PHASTER MEAN BETTER, Clinical chemistry, 43(3), 1997, pp. 424-426
MULTIGENIC INHERITANCE OF HIRSCHSPRUNG-DISEASE
Authors: BOLK S PELET A HOFSTRA RMW SALOMON B ANGRIST M BUYS CHCM LYONNET S CHAKRAVARTI A
Citation: S. Bolk et al., MULTIGENIC INHERITANCE OF HIRSCHSPRUNG-DISEASE, American journal of human genetics, 61(4), 1997, pp. 215-215
GENOMIC ORGANIZATION OF RET-SIGNALING PATHWAY GENES AND MUTATION ANALYSIS IN HIRSCHSPRUNG-DISEASE PATIENTS
Authors: ANGRIST M JING S HALUSHKA M BENTLEY K BOLK S NALLASAMY S FOX GM CHAKRAVARTI A
Citation: M. Angrist et al., GENOMIC ORGANIZATION OF RET-SIGNALING PATHWAY GENES AND MUTATION ANALYSIS IN HIRSCHSPRUNG-DISEASE PATIENTS, American journal of human genetics, 61(4), 1997, pp. 1770-1770
GERMLINE MUTATIONS IN GLIAL-CELL LINE-DERIVED NEUROTROPHIC FACTOR (GDNF) AND RET IN A HIRSCHSPRUNG DISEASE PATIENT
Authors: ANGRIST M BOLK S HALUSHKA M LAPCHAK PA CHAKRAVARTI A
Citation: M. Angrist et al., GERMLINE MUTATIONS IN GLIAL-CELL LINE-DERIVED NEUROTROPHIC FACTOR (GDNF) AND RET IN A HIRSCHSPRUNG DISEASE PATIENT, Nature genetics, 14(3), 1996, pp. 341-344
ENDOTHELIN-3 FRAMESHIFT MUTATION IN CONGENITAL CENTRAL HYPOVENTILATION SYNDROME
Authors: BOLK S ANGRIST M XIE J YANAGISAWA M SILVESTRI JM WEESEMAYER DE CHAKRAVARTI A
Citation: S. Bolk et al., ENDOTHELIN-3 FRAMESHIFT MUTATION IN CONGENITAL CENTRAL HYPOVENTILATION SYNDROME, Nature genetics, 13(4), 1996, pp. 395-396
A HOMOZYGOUS MUTATION IN THE ENDOTHELIN-3 GENE ASSOCIATED WITH A COMBINED WAARDENBURG TYPE-2 AND HIRSCHSPRUNG PHENOTYPE (SHAH-WAARDENBURG SYNDROME)
Authors: HOFSTRA RMW OSINGA J TANSINDHUNATA G WU Y KAMSTEEG EJ STULP RP VANRAVENSWAAIJARTS C MAJOORKRAKAUER D ANGRIST M CHAKRAVARTI A MEIJERS C BUYS CHCM
Citation: Rmw. Hofstra et al., A HOMOZYGOUS MUTATION IN THE ENDOTHELIN-3 GENE ASSOCIATED WITH A COMBINED WAARDENBURG TYPE-2 AND HIRSCHSPRUNG PHENOTYPE (SHAH-WAARDENBURG SYNDROME), Nature genetics, 12(4), 1996, pp. 445-447
CONGENITAL CENTRAL HYPOVENTILATION SYNDROME - MUTATION ANALYSIS OF THE RECEPTOR TYROSINE KINASE RET
Authors: BOLK S ANGRIST M SCHWARTZ S SILVESTRI JM WEESEMAYER DE CHAKRAVARTI A
Citation: S. Bolk et al., CONGENITAL CENTRAL HYPOVENTILATION SYNDROME - MUTATION ANALYSIS OF THE RECEPTOR TYROSINE KINASE RET, American journal of medical genetics, 63(4), 1996, pp. 603-609
MUTATION ANALYSIS OF THE RET RECEPTOR TYROSINE KINASE IN HIRSCHSPRUNGDISEASE
Authors: ANGRIST M BOLK S THIEL B PUFFENBERGER EG HOFSTRA RM BUYS CHCM CASS DT CHAKRAVARTI A
Citation: M. Angrist et al., MUTATION ANALYSIS OF THE RET RECEPTOR TYROSINE KINASE IN HIRSCHSPRUNGDISEASE, Human molecular genetics, 4(5), 1995, pp. 821-830
CHROMOSOMAL LOCALIZATION OF THE MOUSE SRC-LIKE ADAPTER PROTEIN (SLAP)GENE AND ITS PUTATIVE HUMAN HOMOLOG SLA
Authors: ANGRIST M WELLS DE CHAKRAVARTI A PANDEY A
Citation: M. Angrist et al., CHROMOSOMAL LOCALIZATION OF THE MOUSE SRC-LIKE ADAPTER PROTEIN (SLAP)GENE AND ITS PUTATIVE HUMAN HOMOLOG SLA, Genomics, 30(3), 1995, pp. 623-625
MUTATION SCREENING OF THE RET, EDNRB AND ET3 GENES IN HIRSCHSPRUNG PATIENTS
Authors: HOFSTRA RMW ANGRIST M OSINGA J STULP RP TAN G KAMSTEEG EJ SCHEFFER H CHAKRAVARTI A BUYS CHCM
Citation: Rmw. Hofstra et al., MUTATION SCREENING OF THE RET, EDNRB AND ET3 GENES IN HIRSCHSPRUNG PATIENTS, American journal of human genetics, 57(4), 1995, pp. 1110-1110
IDENTITY-BY-DESCENT AND ASSOCIATION MAPPING OF A RECESSIVE GENE FOR HIRSCHSPRUNG DISEASE ON HUMAN-CHROMOSOME 13Q22
Authors: PUFFENBERGER EG KAUFFMAN ER BOLK S MATISE TC WASHINGTON SS ANGRIST M WEISSENBACH J GARVER KL MASCARI M LADDA R SLAUGENHAUPT SA CHAKRAVARTI A
Citation: Eg. Puffenberger et al., IDENTITY-BY-DESCENT AND ASSOCIATION MAPPING OF A RECESSIVE GENE FOR HIRSCHSPRUNG DISEASE ON HUMAN-CHROMOSOME 13Q22, Human molecular genetics, 3(8), 1994, pp. 1217-1225
A GENE FOR HIRSCHSPRUNG DISEASE (MEGACOLON) IN THE PERICENTROMERIC REGION OF HUMAN CHROMOSOME-10
Authors: ANGRIST M KAUFFMAN E SLAUGENHAUPT SA MATISE TC PUFFENBERGER EG WASHINGTON SS LIPSON A CASS DT REYNA T WEEKS DE SIEBER W CHAKRAVARTI A
Citation: M. Angrist et al., A GENE FOR HIRSCHSPRUNG DISEASE (MEGACOLON) IN THE PERICENTROMERIC REGION OF HUMAN CHROMOSOME-10, Nature genetics, 4(4), 1993, pp. 351-356
A GENETIC-LOCUS FOR HIRSCHSPRUNG DISEASE IN THE PERICENTROMERIC REGION OF CHROMOSOME-10
Authors: ANGRIST M KAUFFMAN E MATISE TC SLAUGENHAUPT SA BOLK S PUFFENBERGER EG LIPSON A CASS DT REYNA T WEEKS DE WEISSENBACH J CHAKRAVARTI A
Citation: M. Angrist et al., A GENETIC-LOCUS FOR HIRSCHSPRUNG DISEASE IN THE PERICENTROMERIC REGION OF CHROMOSOME-10, American journal of human genetics, 53(3), 1993, pp. 134-134
IDENTITY-BY-DESCENT MAPPING OF HIRSCHSPRUNG DISEASE IN A LARGE MENNONITE KINDRED
Authors: PUFFENBERGER EG KAUFFMAN ER BOLK S ANGRIST M MATISE TC CHAKRAVARTI A
Citation: Eg. Puffenberger et al., IDENTITY-BY-DESCENT MAPPING OF HIRSCHSPRUNG DISEASE IN A LARGE MENNONITE KINDRED, American journal of human genetics, 53(3), 1993, pp. 1062-1062
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