Richardson AL - Search Results

1

Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP).

Villablanca A, Calender A, Forsberg L, Höög A, Cheng JD, Petillo D, Bauters C, Kahnoski K, Ebeling T, Salmela P, Richardson AL, Delbridge L, Meyrier A, Proye C, Carpten JD, Teh BT, Robinson BG, Larsson C. Villablanca A, et al. Among authors: richardson al. J Med Genet. 2004 Mar;41(3):e32. doi: 10.1136/jmg.2003.012369. J Med Genet. 2004. PMID: 14985403 Free PMC article. No abstract available.

2

Male breast cancer in Cowden syndrome patients with germline PTEN mutations.

Fackenthal JD, Marsh DJ, Richardson AL, Cummings SA, Eng C, Robinson BG, Olopade OI. Fackenthal JD, et al. Among authors: richardson al. J Med Genet. 2001 Mar;38(3):159-64. doi: 10.1136/jmg.38.3.159. J Med Genet. 2001. PMID: 11238682 Free PMC article.

3

Genetic analysis of lithium-associated parathyroid tumors.

Dwight T, Kytölä S, Teh BT, Theodosopoulos G, Richardson AL, Philips J, Twigg S, Delbridge L, Marsh DJ, Nelson AE, Larsson C, Robinson BG. Dwight T, et al. Among authors: richardson al. Eur J Endocrinol. 2002 May;146(5):619-27. doi: 10.1530/eje.0.1460619. Eur J Endocrinol. 2002. PMID: 11980616

4

Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinoma.

Marsh DJ, Learoyd DL, Andrew SD, Krishnan L, Pojer R, Richardson AL, Delbridge L, Eng C, Robinson BG. Marsh DJ, et al. Among authors: richardson al. Clin Endocrinol (Oxf). 1996 Mar;44(3):249-57. doi: 10.1046/j.1365-2265.1996.681503.x. Clin Endocrinol (Oxf). 1996. PMID: 8729519

5

Loss of heterozygosity in sporadic parathyroid tumours: involvement of chromosome 1 and the MEN1 gene locus in 11q13.

Dwight T, Twigg S, Delbridge L, Wong FK, Farnebo F, Richardson AL, Nelson A, Zedenius J, Philips J, Larsson C, Teh BT, Robinson B. Dwight T, et al. Among authors: richardson al. Clin Endocrinol (Oxf). 2000 Jul;53(1):85-92. doi: 10.1046/j.1365-2265.2000.01010.x. Clin Endocrinol (Oxf). 2000. PMID: 10931084

6

Genetic testing for familial cancer. Consequences of RET proto-oncogene mutation analysis in multiple endocrine neoplasia, type 2.

Learoyd DL, Marsh DJ, Richardson AL, Twigg SM, Delbridge L, Robinson BG. Learoyd DL, et al. Among authors: richardson al. Arch Surg. 1997 Sep;132(9):1022-5. doi: 10.1001/archsurg.1997.01430330088015. Arch Surg. 1997. PMID: 9301617

7

Sporadic and familial pheochromocytomas are associated with loss of at least two discrete intervals on chromosome 1p.

Benn DE, Dwight T, Richardson AL, Delbridge L, Bambach CP, Stowasser M, Gordon RD, Marsh DJ, Robinson BG. Benn DE, et al. Among authors: richardson al. Cancer Res. 2000 Dec 15;60(24):7048-51. Cancer Res. 2000. PMID: 11156410

8

A rapid screening method for the detection of mutations in the RET proto-oncogene in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma families.

Marsh DJ, Robinson BG, Andrew S, Richardson AL, Pojer R, Schnitzler M, Mulligan LM, Hyland VJ. Marsh DJ, et al. Among authors: richardson al. Genomics. 1994 Sep 15;23(2):477-9. doi: 10.1006/geno.1994.1526. Genomics. 1994. PMID: 7835899

9

Rapid mutation scanning of genes associated with familial cancer syndromes using denaturing high-performance liquid chromatography.

Marsh DJ, Theodosopoulos G, Howell V, Richardson AL, Benn DE, Proos AL, Eng C, Robinson BG. Marsh DJ, et al. Among authors: richardson al. Neoplasia. 2001 May-Jun;3(3):236-44. doi: 10.1038/sj.neo.7900154. Neoplasia. 2001. PMID: 11494117 Free PMC article.

10

MEN type 2a presenting as an intra-abdominal emergency.

Evans JP, Bambach CP, Andrew S, Dwight T, Richardson AL, Robinson BG, Delbridge L. Evans JP, et al. Among authors: richardson al. Aust N Z J Surg. 1997 Nov;67(11):824-6. doi: 10.1111/j.1445-2197.1997.tb04599.x. Aust N Z J Surg. 1997. PMID: 9397010 No abstract available.

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