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Results: 1-10 |
Results: 10
GNAS1 MUTATIONAL ANALYSIS IN PSEUDOHYPOPARATHYROIDISM
Authors: AHMED SF DIXON PH BONTHRON DT STIRLING HF BARR DGD KELNAR CJH THAKKER RV
Citation: Sf. Ahmed et al., GNAS1 MUTATIONAL ANALYSIS IN PSEUDOHYPOPARATHYROIDISM, Clinical endocrinology, 49(4), 1998, pp. 525-531
LOCALIZATION OF X-LINKED RECESSIVE IDIOPATHIC HYPOPARATHYROIDISM TO A1.5 MB REGION ON XQ26-Q27
Authors: TRUMP D DIXON PH MUMM S WOODING C DAVIES KE SCHLESSINGER D WHYTE MP THAKKER RV
Citation: D. Trump et al., LOCALIZATION OF X-LINKED RECESSIVE IDIOPATHIC HYPOPARATHYROIDISM TO A1.5 MB REGION ON XQ26-Q27, Journal of Medical Genetics, 35(11), 1998, pp. 905-909
MUTATIONAL ANALYSIS OF PHEX GENE IN X-LINKED HYPOPHOSPHATEMIA
Authors: DIXON PH CHRISTIE PT WOODING C TRUMP D GRIEFF M HOLM I GERTNER JM SCHMIDTKE J SHAH B SHAW N SMITH C TAU C SCHLESSINGER D WHYTE MP THAKKER RV
Citation: Ph. Dixon et al., MUTATIONAL ANALYSIS OF PHEX GENE IN X-LINKED HYPOPHOSPHATEMIA, The Journal of clinical endocrinology and metabolism, 83(10), 1998, pp. 3615-3623
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
MUTATIONS OF THE PEX REGULATORY AND C-TERMINAL REGIONS CAUSE X-LINKEDHYPOPHOSPHATEMIA
Authors: DIXON PH WOODING C CHRISTIE P GRIEFF M SCHLESSINGER D WHYTE MP THAKKER RV
Citation: Ph. Dixon et al., MUTATIONS OF THE PEX REGULATORY AND C-TERMINAL REGIONS CAUSE X-LINKEDHYPOPHOSPHATEMIA, Journal of bone and mineral research, 12, 1997, pp. 101-101
X-LINKED HYPOPHOSPHATEMIC RICKETS IN A SAUDI-ARABIAN KINDRED RESULTS FROM A NONSENSE MUTATION OF THE PEX GENE
Authors: DIXON PH WOODING C CRISTIE P THAKKER RV
Citation: Ph. Dixon et al., X-LINKED HYPOPHOSPHATEMIC RICKETS IN A SAUDI-ARABIAN KINDRED RESULTS FROM A NONSENSE MUTATION OF THE PEX GENE, Journal of bone and mineral research, 12, 1997, pp. 528-528
7 NOVEL MUTATIONS IN THE PEX GENE INDICATE MOLECULAR HETEROGENEITY FOR X-LINKED HYPOPHOSPHATEMIC RICKETS
Authors: DIXON PH WOODING C TRUMP D SCHLESSINGER D WHYTE MP THAKKER RV
Citation: Ph. Dixon et al., 7 NOVEL MUTATIONS IN THE PEX GENE INDICATE MOLECULAR HETEROGENEITY FOR X-LINKED HYPOPHOSPHATEMIC RICKETS, Journal of bone and mineral research, 11, 1996, pp. 165-165
GENETIC-MAPPING STUDIES OF THE X-LINKED RECESSIVE HYPOPARATHYROID GENE ON THE X-CHROMOSOME (XQ27)
Authors: DIXON PH TRUMP D WOODING C MUMM S SCHLESSINGER D WHYTE MP THAKKER RV
Citation: Ph. Dixon et al., GENETIC-MAPPING STUDIES OF THE X-LINKED RECESSIVE HYPOPARATHYROID GENE ON THE X-CHROMOSOME (XQ27), Journal of bone and mineral research, 11, 1996, pp. 169-169
MUTATIONAL ANALYSIS OF THE GNAS1 GENE IN PSEUDOHYPOPARATHYROIDISM
Authors: DIXON PH AHMED SF BONTHRON DT BARR DGD KELNAR CJH THAKKER RV
Citation: Ph. Dixon et al., MUTATIONAL ANALYSIS OF THE GNAS1 GENE IN PSEUDOHYPOPARATHYROIDISM, Journal of bone and mineral research, 11, 1996, pp. 494-494
CONSTRUCTION OF A YAC CONTIG AND AN STS MAP SPANNING 3.6 MEGABASE PAIRS IN XP22.1
Authors: TRUMP D PILIA G DIXON PH WOODING C THAKRAR R LEIGH SEA NAGARAJA R WHYTE MP SCHLESSINGER D THAKKER RV
Citation: D. Trump et al., CONSTRUCTION OF A YAC CONTIG AND AN STS MAP SPANNING 3.6 MEGABASE PAIRS IN XP22.1, Human genetics, 97(1), 1996, pp. 60-68
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