AAAAAA

   
Results: 1-18 |
Results: 18
A NOVEL INTEGRATED SILICON CAPACITIVE MICROPHONE - FLOATING ELECTRODEELECTRET MICROPHONE (FEEM)
Authors: ZOU QB TAN ZM WANG ZF PANG JT QIAN X ZHANG QX LIN RM YI S GONG HQ LIU LT LI ZJ
Citation: Qb. Zou et al., A NOVEL INTEGRATED SILICON CAPACITIVE MICROPHONE - FLOATING ELECTRODEELECTRET MICROPHONE (FEEM), Journal of microelectromechanical systems, 7(2), 1998, pp. 224-234
LINKAGE STUDIES OF A MISSOURI KINDRED WITH AUTOSOMAL-DOMINANT SPONDYLOEPIMETAPHYSEAL DYSPLASIA (SEMD) INDICATE GENETIC-HETEROGENEITY
Authors: GERTNER JM WHYTE MP DIXON PH PANG JT TRUMP D PEARCE SHS WOODING C THAKKER RV
Citation: Jm. Gertner et al., LINKAGE STUDIES OF A MISSOURI KINDRED WITH AUTOSOMAL-DOMINANT SPONDYLOEPIMETAPHYSEAL DYSPLASIA (SEMD) INDICATE GENETIC-HETEROGENEITY, Journal of bone and mineral research, 12(8), 1997, pp. 1204-1209
EXCLUSION OF ZFM1 AS A CANDIDATE GENE FOR MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 (MEN1)
Authors: LLOYD SE PANG JT PEARCE SHS LEIGH SEA THAKKER RV
Citation: Se. Lloyd et al., EXCLUSION OF ZFM1 AS A CANDIDATE GENE FOR MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 (MEN1), Human genetics, 99(5), 1997, pp. 585-589
LOCALIZATION OF A GENE CAUSING ENDOCRINE NEOPLASIA TO A 4-CM REGION ON CHROMOSOME 1P35-P36
Authors: WILLIAMSON C PANNETT AAJ PANG JT WOODING C MCCARTHY M SHEPPARD MN MONSON J CLAYTON RN THAKKER RV
Citation: C. Williamson et al., LOCALIZATION OF A GENE CAUSING ENDOCRINE NEOPLASIA TO A 4-CM REGION ON CHROMOSOME 1P35-P36, Journal of Medical Genetics, 34(8), 1997, pp. 617-619
CLINICAL-STUDIES OF MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 (MEN1)
Authors: TRUMP D FARREN B WOODING C PANG JT BESSER GM BUCHANAN KD EDWARDS CR HEATH DA JACKSON CE JANSEN S LIPS K MONSON JP OHALLORAN D SAMPSON J SHALET SM WHEELER MH ZINK A THAKKER RV
Citation: D. Trump et al., CLINICAL-STUDIES OF MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 (MEN1), Quarterly Journal of Medicine, 89(9), 1996, pp. 653-669
CLINICAL-STUDIES OF MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 (MEN1) (VOL 89, PG 653, 1996)
Authors: TRUMP D FARREN B WOODING C PANG JT BESSER GM BUCHANAN KD EDWARDS CR HEATH DA JACKSON CE JANSEN S LIPS K MONSON JP OHALLORAN D SAMPSON J SHALET SM WHEELER MH ZINK A THAKKER RV
Citation: D. Trump et al., CLINICAL-STUDIES OF MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 (MEN1) (VOL 89, PG 653, 1996), Quarterly Journal of Medicine, 89(12), 1996, pp. 957-958
GENETIC-MAPPING STUDIES OF 40 LOCI AND 23 COSMIDS IN CHROMOSOME-11P13-11Q13, AND EXCLUSION OF MU-CALPAIN AS THE MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 GENE
Authors: PANG JT LLOYD SE WOODING C FARREN B POTTINGER B HARDING B LEIGH SEA POOK MA BENHAM FJ GILLETT GT TAGGART RT THAKKER RV
Citation: Jt. Pang et al., GENETIC-MAPPING STUDIES OF 40 LOCI AND 23 COSMIDS IN CHROMOSOME-11P13-11Q13, AND EXCLUSION OF MU-CALPAIN AS THE MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 GENE, Human genetics, 97(6), 1996, pp. 732-741
REFINED LOCALIZATION OF THE DARIERS-DISEASE AND SPINOCEREBELLAR ATAXIA TYPE-2 GENES AT CHROMOSOME 12Q24.1 - CONSTRUCTION OF A YAC CONTIG ENCOMPASSING THESE GENES
Authors: BRYCE SD CARTER SA PANG JT TWELLS R RENAULT B SCHLEICHNORTE B ALLOTEY R ROSS CJD KATSANTONIA E WEISSENBACH J KUCHERLAPATI RS REES JL MUNRO CS CHAMBERLAIN S STRACHAN T
Citation: Sd. Bryce et al., REFINED LOCALIZATION OF THE DARIERS-DISEASE AND SPINOCEREBELLAR ATAXIA TYPE-2 GENES AT CHROMOSOME 12Q24.1 - CONSTRUCTION OF A YAC CONTIG ENCOMPASSING THESE GENES, Journal of investigative dermatology, 107(3), 1996, pp. 210-210
LOCALIZATION OF A TUMOR-SUPPRESSOR GENE CAUSING PARATHYROID TUMORS TOCHROMOSOME-1P34-P36
Authors: WILLIAMSON C PANNETT A PANG JT MCCARTHY M MONSON JP THAKKER RV
Citation: C. Williamson et al., LOCALIZATION OF A TUMOR-SUPPRESSOR GENE CAUSING PARATHYROID TUMORS TOCHROMOSOME-1P34-P36, Journal of bone and mineral research, 10, 1995, pp. 154-154
LINKAGE STUDIES IN A KINDRED FROM OKLAHOMA, WITH FAMILIAL BENIGN (HYPOCALCIURIC) HYPERCALCEMIA (FBH) AND DEVELOPMENTAL ELEVATIONS IN SERUM PARATHYROID-HORMONE LEVELS, INDICATE A 3RD LOCUS FOR FBH
Authors: TRUMP D WHYTE MP WOODING C PANG JT PEARCE SHS KOCHER DB THAKKER RV
Citation: D. Trump et al., LINKAGE STUDIES IN A KINDRED FROM OKLAHOMA, WITH FAMILIAL BENIGN (HYPOCALCIURIC) HYPERCALCEMIA (FBH) AND DEVELOPMENTAL ELEVATIONS IN SERUM PARATHYROID-HORMONE LEVELS, INDICATE A 3RD LOCUS FOR FBH, Human genetics, 96(2), 1995, pp. 183-187
LINKAGE STUDIES IN A KINDRED FROM OKLAHOMA WITH FAMILIAL BENIGN HYPOCALCIURIC HYPERCALCEMIA (FBH) INDICATE GENETIC-HETEROGENEITY AND A 3RD LOCUS FOR FBH
Authors: TRUMP D WHYTE MP WOODING C PANG JT KOCHER D THAKKER RV
Citation: D. Trump et al., LINKAGE STUDIES IN A KINDRED FROM OKLAHOMA WITH FAMILIAL BENIGN HYPOCALCIURIC HYPERCALCEMIA (FBH) INDICATE GENETIC-HETEROGENEITY AND A 3RD LOCUS FOR FBH, Journal of Medical Genetics, 32(2), 1995, pp. 152-152
CONSTRUCTION OF A 2.4 MEGABASE YAC CONTIG ENCOMPASSING THE SCA2 CRITICAL REGION ON CHROMOSOME 12Q23-24.1
Authors: TWELLS R PANG JT ALLOTEY R NORTE BS BRYCE S WILLIAMSON R CHAMBERLAIN S
Citation: R. Twells et al., CONSTRUCTION OF A 2.4 MEGABASE YAC CONTIG ENCOMPASSING THE SCA2 CRITICAL REGION ON CHROMOSOME 12Q23-24.1, American journal of human genetics, 57(4), 1995, pp. 1582-1582
MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 (MEN1)
Authors: PANG JT THAKKER RV
Citation: Jt. Pang et Rv. Thakker, MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 (MEN1), European journal of cancer, 30A(13), 1994, pp. 1961-1968
MAPPING OF 2 HEREDITARY RENAL TUBULAR DISORDERS ASSOCIATED WITH KIDNEY-STONES, AND REFERRED TO AS DENT-DISEASE AND X-LINKED RECESSIVE NEPHROLITHIASIS, TO CHROMOSOME-XP11
Authors: THAKKER RV PANG JT WOODING C SCHEINMAN SJ WRONG OM POOK MA
Citation: Rv. Thakker et al., MAPPING OF 2 HEREDITARY RENAL TUBULAR DISORDERS ASSOCIATED WITH KIDNEY-STONES, AND REFERRED TO AS DENT-DISEASE AND X-LINKED RECESSIVE NEPHROLITHIASIS, TO CHROMOSOME-XP11, Cytogenetics and cell genetics, 67(4), 1994, pp. 352-352
MOLECULAR-GENETIC MAPPING OF 13 MARKERS FROM CHROMOSOME-11Q13 IN 33 FAMILIES WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE-1
Authors: PANG JT WOODING C LEIGH SEA TAGGART RT SHEFFIELD V JONES C THAKKER RV
Citation: Jt. Pang et al., MOLECULAR-GENETIC MAPPING OF 13 MARKERS FROM CHROMOSOME-11Q13 IN 33 FAMILIES WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE-1, Journal of bone and mineral research, 8, 1993, pp. 190000136-190000136
LINKAGE STUDIES IN A KINDRED WITH HYPOCALCIURIC HYPERCALCEMIA AND INCREASING SERUM PARATHYROID-HORMONE LEVELS INDICATE GENETIC-HETEROGENEITY
Authors: TRUMP D WHYTE MP WOODING C PANG JT KOCHER D THAKKER RV
Citation: D. Trump et al., LINKAGE STUDIES IN A KINDRED WITH HYPOCALCIURIC HYPERCALCEMIA AND INCREASING SERUM PARATHYROID-HORMONE LEVELS INDICATE GENETIC-HETEROGENEITY, Journal of bone and mineral research, 8, 1993, pp. 190000167-190000167
MAPPING THE GENE CAUSING X-LINKED RECESSIVE NEPHROLITHIASIS TO XP11.22 BY LINKAGE STUDIES
Authors: SCHEINMAN SJ POOK MA WOODING C PANG JT FRYMOYER PA THAKKER RV
Citation: Sj. Scheinman et al., MAPPING THE GENE CAUSING X-LINKED RECESSIVE NEPHROLITHIASIS TO XP11.22 BY LINKAGE STUDIES, The Journal of clinical investigation, 91(6), 1993, pp. 2351-2357
LINKAGE ANALYSIS OF 7-POLYMORPHIC MARKERS AT CHROMOSOME 11P11.2-11Q13IN 27 MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 FAMILIES
Authors: THAKKER RV WOODING C PANG JT FARREN B HARDING B ANDERSON DC BESSER GM BOULOUX P BRENTON DP BUCHANAN KD EDWARDS CR HEATH DA JACKSON CE JANSEN S LIPS K NORUM RA SAMPSON J SHALET SM TAGGART RT TAILOR D WHEELER MH WOOLLARD PM YATES J
Citation: Rv. Thakker et al., LINKAGE ANALYSIS OF 7-POLYMORPHIC MARKERS AT CHROMOSOME 11P11.2-11Q13IN 27 MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 FAMILIES, Annals of Human Genetics, 57, 1993, pp. 17-25
Risultati: 1-18 |