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| 1 | Characterization of GATA3 mutations in the hypoparathyroidism,deafness,and renal dysplasia (HDR) syndrome显示文摘 | Nesbit MA Bowl MR Harding B | 2004 | J Biol Chem2004，279，22： | 1 |
| 2 | GATA3 haplo-insufficiency causes human HDR syndrome显示文摘 | Van Esch H Groenen P Nesbit MA | 2000 | Nature2000，406，： | 1 |
| 3 | A missense glial cells missing homolog B (GCMB) mutation, AsnSO2His, causes autosomal dominant hypoparathyroidism显示文摘 | Mirczuk SM Bowl MR Nesbit MA | 2010 | J Clin Endocrinol Metab2010，95，7： | 1 |
| 4 | A missense GATA3mutation, Thr272Ile, causes the hypoparathyroidism, deafness, andrenal dysplasia syndrome 显示文摘 | Gaynor KU Grigorieva IV Nesbit MA | 2009 | J Clin Endocrinol Metab2009，94，10： | 1 |
| 5 | GATA3 haplo-insufflciency causes human HDR syndrome 显示文摘 | Van Escb H Groenen P Nesbit MA | 2000 | Nature2000，406，6794： | 1 |
| 6 | Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3显示文摘 | Nesbit MA Hannan FM Howles SA | 2013 | Nat Genet2013，45，： | 1 |
| 7 | Mutations affecting G-protein subunit alpha11 in hypercalcemia and hypocalcemia显示文摘 | Nesbit MA Hannan FM Howles SA | 2013 | N Engl J Med2013，368，： | 1 |
| 8 | Mutational analysis in X-linked spondyloepiphyseal dysplasia tarda显示文摘 | CHRISTIE PT CURLEY A NESBIT MA | 2001 | The Journal of Clinical Endocrinology and Metabolism2001，86，7： | 1 |
| 9 | Mutation analysis in X-linked spondyloepiphyseal dysplasia tarda显示文摘 | Christie PT Curley A Nesbit MA | 2001 | Clin Endocrinol Metab2001，86，7： | 1 |
| 10 | A homozygous inactivating calcium-sensing receptor mutation,Pro339Thr,is associated with isolated primary hyperparathyroidism:correlation between location of mutations and severity of hypercalcaemia显示文摘 | HANNAN FM NESBIT MA CHRISTIE PT | 2010 | Clin Endocrinol(Oxf)2010，73，6： | 1 |
| 11 | Hepatitis B surface antigenemia iollowing recombinantEngerix B hepatitis B vaccine in an 81-year-oidESRD patient on hemodialysis 显示文摘 | ONUIGBO MA NESBIT A WEISENBECK J | 2010 | Ren Fail2010，32，4： | 1 |
| 12 | Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome显示文摘 | Nesbit MA Bowl MR Harding B | 2004 | Biological Chemistry2004，279，22： | 1 |
| 13 | GATA3 haplo-insufficient'ycauses human HDR syndrome 显示文摘 | Van Esch H Groenen P Nesbit MA | 2000 | Nature2000，406，6794： | 1 |
| 14 | Functional analysis of a novelGAT A3 mutation in a family with the hypoparathyroidism,deafness,and renal dysplasia syndrome显示文摘 | Zahirieh A Nesbit MA Ali A | 2005 | J Clin Endocrinol Metab2005，90，4： | 1 |
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