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Results: 26-50/117
Authors:
CARRASQUILLO MM
ZLOTOGORA J
CHAKRAVARTI A
Citation: Mm. Carrasquillo et al., 2 CONNEXIN-26 MUTATIONS OF RECENT ORIGIN SEGREGATING IN A SINGLE INBRED KINDRED WITH NONSYNDROMIC RECESSIVE DEAFNESS, American journal of human genetics, 61(4), 1997, pp. 143-143
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
Authors:
HONG HK
BENTLEY K
CHAKRAVARTI A
Citation: Hk. Hong et al., FINE-STRUCTURE MAPPING OF CONGENITAL HYDROCEPHALUS (CH) - A MOUSE MODEL FOR HUMAN HYDROCEPHALUS, American journal of human genetics, 61(4), 1997, pp. 880-880
Authors:
MATISE TC
KASHUK C
THANGARAJAH T
CHAKRAVARTI A
JAMES M
Citation: Tc. Matise et al., COMBINING RADIATION HYBRID PANELS TO INCREASE MAPPING POWER, American journal of human genetics, 61(4), 1997, pp. 1386-1386
Authors:
NATH SK
CHAKRAVARTI A
Citation: Sk. Nath et A. Chakravarti, THE ASSESSMENT OF SIBLING RELATIONSHIP, American journal of human genetics, 61(4), 1997, pp. 1675-1675
Authors:
PULVER AE
ANTONARAKIS SE
BLOUIN JL
GEHRIG C
RADHAKVISHNA U
LOETSCHER E
KAZAZIAN HH
DOMBROSKI B
LASSETER VK
NESTADT G
NATH S
CHAKRAVARTI A
DEMARCHI N
HOUSMAN D
WOLYNIEC P
Citation: Ae. Pulver et al., A GENOME SEARCH FOR SCHIZOPHRENIA SUSCEPTIBILITY LOCI - SIB-PAIR SHARING OF ALLELES ON CHROMOSOME 5Q22-5Q31 IN 54 PEDIGREES, American journal of human genetics, 61(4), 1997, pp. 1701-1701
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
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
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
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
Authors:
BOGUSKI M
CHAKRAVARTI A
GIBBS R
GREEN E
MYERS RM
Citation: M. Boguski et al., THE END OF THE BEGINNING - THE RACE TO BEGIN HUMAN GENOME SEQUENCING, PCR methods and applications, 6(9), 1996, pp. 771-772
Authors:
BOGUSKI M
CHAKRAVARTI A
GIBBS R
GREEN E
MYERS R
Citation: M. Boguski et al., UNTITLED, PCR methods and applications, 6(1), 1996, pp. 5-5
Authors:
CHAKRAVARTI A
Citation: A. Chakravarti, ENDOTHELIN RECEPTOR-MEDIATED SIGNALING IN HIRSCHSPRUNG DISEASE, Human molecular genetics, 5(3), 1996, pp. 303-307
Authors:
EICHLER EE
MACPHERSON JN
MURRAY A
JACOBS PA
CHAKRAVARTI A
NELSON DL
Citation: Ee. Eichler et al., HAPLOTYPE AND INTERSPERSION ANALYSIS OF THE FMR1 CGG REPEAT IDENTIFIES 2 DIFFERENT MUTATIONAL PATHWAYS FOR THE ORIGIN OF THE FRAGILE-X SYNDROME, Human molecular genetics, 5(3), 1996, pp. 319-330
Authors:
MATISE TC
SHAW SH
CHAKRAVARTI A
Citation: Tc. Matise et al., AUTOMATED RADIATION HYBRID MAPPING ON CHROMOSOME-13, Cytogenetics and cell genetics, 75(2-3), 1996, pp. 108-108
Authors:
SOARES MB
BONALDO MF
JELENC P
LAWTON L
VENKATRAJ VS
WASHINGTON S
WELLINGTON S
CHAKRAVARTI A
WARBURTON D
Citation: Mb. Soares et al., IDENTIFICATION AND MAPPING OF OVER 100 GENES ON HUMAN-CHROMOSOME-13, Cytogenetics and cell genetics, 75(2-3), 1996, pp. 109-109
Authors:
CHAKRAVARTI A
BLANTON S
KENDALL BJ
MCCALLUM RW
Citation: A. Chakravarti et al., COSEGREGATION OF FAMILIAL INTESTINAL PSEUDOOBSTRUCTION AND PRESENCE OF DIGITAL ARCHES IN A LARGE MULTIGENERATIONAL PEDIGREE, Digestive diseases and sciences, 41(7), 1996, pp. 1429-1433
Authors:
NIMGAONKAR VL
SANDERS AR
GANGULI R
ZHANG XR
BRAR J
HOGGE W
FANN WE
PATEL PI
CHAKRAVARTI A
Citation: Vl. Nimgaonkar et al., ASSOCIATION STUDY OF SCHIZOPHRENIA AND THE DOPAMINE D3 RECEPTOR GENE LOCUS IN 2 INDEPENDENT SAMPLES, American journal of medical genetics, 67(6), 1996, pp. 505-514
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
Authors:
RAY A
CHAKRAVARTI A
RANGANATHAN R
Citation: A. Ray et al., AN AUTOMATED MAGNETOMETER USING THE CHEBYSHEV METHOD OF NUMERICAL-INTEGRATION, Review of scientific instruments, 67(3), 1996, pp. 789-795
Authors:
STRASS E
MCCABE ERB
BIESECKER L
CASSIDY S
CHAKRAVARTI A
GRODY W
JUENGST E
KHORY M
KNOPPERS BM
MOTULSKY A
PHILLIPS JA
SPENCE MA
Citation: E. Strass et al., ASHG REPORT - STATEMENT ON INFORMED CONSENT FOR GENETIC RESEARCH, American journal of human genetics, 59(2), 1996, pp. 471-474
Authors:
CHEN HM
ROSSIER C
LALIOTI MD
LYNN A
CHAKRAVARTI A
PERRIN G
ANTONARAKIS SE
Citation: Hm. Chen et al., CLONING OF THE CDNA FOR A HUMAN HOMOLOG OF THE DROSOPHILA WHITE GENE AND MAPPING TO CHROMOSOME 21Q22.3, American journal of human genetics, 59(1), 1996, pp. 66-75
Authors:
KWOH CK
VENGLISH C
LYNN AH
WHITLEY DM
YOUNG E
CHAKRAVARTI A
Citation: Ck. Kwoh et al., AGE, SEX, AND THE FAMILIAL RISK OF RHEUMATOID-ARTHRITIS, American journal of epidemiology, 144(1), 1996, pp. 15-24
Authors:
CHAKRAVARTI A
Citation: A. Chakravarti, THE CD4 CD8 RATIO - MESSAGE IN A BOTTLE, Nature medicine, 1(12), 1995, pp. 1240-1241
Authors:
TALBOT CC
AVRAMOPOULOS D
GERKEN S
CHAKRAVARTI A
ARMOUR JA
MATSUNAMI N
WHITE R
ANTONARAKIS SE
Citation: Cc. Talbot et al., THE TETRANUCLEOTIDE REPEAT POLYMORPHISM D21S1245 DEMONSTRATES HYPERMUTABILITY IN GERMLINE AND SOMATIC-CELLS, Human molecular genetics, 4(7), 1995, pp. 1193-1199