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Results: 1-14 |
Results: 14

Authors: AU KS RODRIGUEZ JA FINCH JL VOLCIK KA ROACH ES DELGADO MR RODRIGUEZ E NORTHRUP H
Citation: Ks. Au et al., GERM-LINE MUTATIONAL ANALYSIS OF THE TSC2 GENE IN 90 TUBEROUS-SCLEROSIS PATIENTS, American journal of human genetics, 62(2), 1998, pp. 286-294

Authors: AU KS RODRIGUEZ JA RODRIGUEZ E DOBYNS WB DELGADO MR NORTHRUP H
Citation: Ks. Au et al., MUTATIONS AND POLYMORPHISMS IN THE TUBEROUS SCLEROSIS COMPLEX GENE ONCHROMOSOME-16, Human mutation, 9(1), 1997, pp. 23-29

Authors: BAUMGARTNER JE WHELESS JW KULKARNI S NORTHRUP H AU KS SMITH A BROOKSHIR B
Citation: Je. Baumgartner et al., ON THE SURGICAL-TREATMENT OF REFRACTORY EPILEPSY IN TUBEROUS SCLEROSIS COMPLEX, Pediatric neurosurgery, 27(6), 1997, pp. 311-318

Authors: FUNG KFLH LEUNG KF SHUM PS AU KS CHAN SP TAY M CHAN CH CHIN PH FONG D WONG A CHENG S LO TC CHAN LW LEUNG SF CHU M LI H KO F CHU M WONG S CHENG S LAU J LEE SW CHAN KS
Citation: Kflh. Fung et al., WHOQOL - THE DEVELOPMENT OF NATIONAL QUESTIONS FOR HONG-KONG, Quality of life research, 6(5), 1997, pp. 144-144

Authors: NORTHRUP H RODRIGUEZ E AU KS BLANTON S DOBYNS WB
Citation: H. Northrup et al., LINKAGE STUDIES OF WALKER-WARBURG SYNDROME (WWS) AND CHROMOSOME 9Q31-32, Annals of Human Genetics, 61, 1997, pp. 218-219

Authors: ROSS VM PRASHNER HR AU KS NORTHRUP H
Citation: Vm. Ross et al., GONADAL MOSAICISM IN TUBEROUS SCLEROSIS, American journal of human genetics, 61(4), 1997, pp. 111-111

Authors: AU KS ROACH ES NORTHRUP H
Citation: Ks. Au et al., A SEVERE RENAL PHENOTYPE RESULTING FROM A TSC2 MUTATION WITHOUT INVOLVEMENT OF THE PKD1 GENE, American journal of human genetics, 61(4), 1997, pp. 1904-1904

Authors: AU KS MURRELL J BUCKLER A BLANTON SH NORTHRUP H
Citation: Ks. Au et al., REPORT OF A CRITICAL RECOMBINATION FURTHER NARROWING THE TSC1 REGION, Journal of Medical Genetics, 33(7), 1996, pp. 559-561

Authors: GREENSPAN DS NORTHRUP H AU KS MCALLISTER KA FRANCOMANO CA WENSTRUP RJ MARCHUK DA KWIATKOWSKI DJ
Citation: Ds. Greenspan et al., COL5A1 - FINE GENETIC-MAPPING AND EXCLUSION AS CANDIDATE GENE IN FAMILIES WITH NAIL-PATELLA SYNDROME, TUBEROUS SCLEROSIS-1, HEREDITARY HEMORRHAGIC TELANGIECTASIA, AND EHLERS-DANLOS SYNDROME TYPE-II, Genomics, 25(3), 1995, pp. 737-739

Authors: AU KS ROACH ES NORTHRUP H
Citation: Ks. Au et al., MUTATIONS OF THE TUBEROUS SCLEROSIS COMPLEX-2 (TSC2) GENE IN AN ISOLATED ANGIOMYOLIPOMA, American journal of human genetics, 57(4), 1995, pp. 307-307

Authors: AU KS
Citation: Ks. Au, DEPENDENCE OF FLUIDITY OF HUMAN ERYTHROCYTE-MEMBRANES ON THEIR METHODS OF PREPARATION, Biochemistry and molecular biology international, 32(1), 1994, pp. 49-53

Authors: AU KS BLANTON SH KWIATKOWSKI DJ NORTHRUP H
Citation: Ks. Au et al., FURTHER NARROWING OF THE REGION ON CHROMOSOME-9Q34 CONTAINING THE TSCGENE, Cytogenetics and cell genetics, 64(2), 1993, pp. 107-107

Authors: AU KS MATTION NM ESTES MK
Citation: Ks. Au et al., A SUBVIRAL PARTICLE BINDING DOMAIN ON THE ROTAVIRUS NONSTRUCTURAL GLYCOPROTEIN-NS28, Virology, 194(2), 1993, pp. 665-673

Authors: AU KS NORTHRUP H
Citation: Ks. Au et H. Northrup, DISPLACEMENT LOOP TRIPLEX AFFINITY CAPTURE OF SEQUENCE-SPECIFIC HIGH-MOLECULAR-WEIGHT (HMW) DNA FOR YAC CLONING, American journal of human genetics, 53(3), 1993, pp. 1267-1267
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