Immunohistochemistry for SDHB triages genetic testing of SDHB , SDHC , and SDHD in paraganglioma-pheochromocytoma syndromes von Gill, Anthony J., FRCPA, Benn, Diana E., PhD, Chou, Angela, FRCPA, Clarkson, Adele, BSc, Muljono, Anita, FRCPA, Meyer-Rochow, Goswin Y., FRACS, Richardson, Anne Louise, BSc, Sidhu, Stan B., PhD, Robinson, Bruce G., MD, Clifton-Bligh, Roderick J., PhD

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Experience of prophylactic thyroidectomy in multiple endocrine neoplasia type 2A kindreds with RET codon 804 mutations von Learoyd, Diana L., Gosnell, Jessica, Elston, Marianne S., Saurine, Tricia J., Richardson, Anne-Louise, Delbridge, Leigh W., Con Aglen, John V., Robinson, Bruce G.

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Denaturing High Performance Liquid Chromatography Detection of SDHB , SDHD , and VHL Germline Mutations in Pheochromocytoma von Meyer-Rochow, Goswin Y., F.R.A.C.S, Smith, Janine M., M.B.Ch.B, Richardson, Anne-Louise, B.Sc, Marsh, Deborah J., Ph.D, Sidhu, Stan B., Ph.D, Robinson, Bruce G., M.D, Benn, Diana E., Ph.D

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Analysis of SDHAF3 in familial and sporadic pheochromocytoma and paraganglioma von Dwight, Trisha, Na, Un, Kim, Edward, Zhu, Ying, Richardson, Anne Louise, Robinson, Bruce G, Tucker, Katherine M, Gill, Anthony J, Benn, Diana E, Clifton-Bligh, Roderick J, Winge, Dennis R

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Mutation Spectrum and Genotype-Phenotype Analyses in Cowden Disease and Bannayan-Zonana Syndrome, Two Hamartoma Syndromes With Germline PTEN Mutation von Marsh, Debbie J., Coulon, Valérie, Lunetta, Kathryn L., Rocca-Serra, Philippe, Dahia, Patricia L. M., Zheng, Zimu, Liaw, Danny, Caron, Stacey, Duboué, Bernadette, Lin, Albert Y., Richardson, Anne-Louise, Bonnetblanc, Jean-Marie, Bressieux, Jean-Marie, Cabarrot-Moreau, Agnés, Chompret, Agnés, Demange, Liliane, Eeles, Rosalind A., Yahanda, Alan M., Fearon, Eric R., Fricker, Jean-Pierre, Gorlin, Robert J., Hodgson, Shirley V., Huson, Susan, Lacombe, Didier, LePrat, Frédéric, Odent, Sylvie, Toulouse, Claude, Olopade, Olufunmilayo I., Sobol, Hagay, Tishler, Sigrid, Woods, C. Geoffrey, Robinson, Bruce G., Weber, H. Christian, Parsons, Ramon, Peacocke, Monica, Longy, Michel, Eng, Charis

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Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas von BENN, Diana E, CROXSON, Michael S, TUCKER, Kathy, BAMBACH, Christopher P, RICHARDSON, Anne Louise, DELBRIDGE, Leigh, PULLAN, Peter T, HAMMOND, Jeremy, MARSH, Deborah J, ROBINSON, Bruce G

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Rapid Mutation Scanning of Genes Associated with Familial Cancer Syndromes Using Denaturing High-Performance Liquid Chromatography von Marsh, Deborah J., Theodosopoulos, George, Howell, Viive, Richardson, Anne-Louise, Benn, Diana E., Proos, Anné L., Eng, Charis, Robinson, Bruce G.

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Genetic Testing in Pheochromocytoma- and Paraganglioma-Associated Syndromes von BENN, DIANA E., RICHARDSON, ANNE LOUISE, MARSH, DEBORAH J., ROBINSON, BRUCE G.

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Genome-Wide Copy Number Imbalances Identified in Familial and Sporadic Medullary Thyroid Carcinoma von Marsh, Deborah J., Theodosopoulos, George, Martin-Schulte, Klaus, Richardson, Anne-Louise, Philips, Jeanette, Röher, Hans-Dietrich, Delbridge, Leigh, Robinson, Bruce G.

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Rapid Mutation Screening for HRPT2 and MEN1 Mutations Associated with Familial and Sporadic Primary Hyperparathyroidism von Howell, Viive M., Cardinal, John W., Richardson, Anne-Louise, Gimm, Oliver, Robinson, Bruce G., Marsh, Deborah J.

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Germline SDHC mutation presenting as recurrent SDH deficient GIST and renal carcinoma von Gill, Anthony J., Lipton, Lara, Taylor, Jessica, Benn, Diane E., Richardson, Anne Louise, Frydenberg, Mark, Shapiro, Jeremy, Clifton-Bligh, Roderick J., Chow, Chung W., Bogwitz, Michael

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Abstract 5597: Targeted massively parallel sequencing for the diagnosis of hereditary neuroendocrine disorders von Dwight, Trish, Richardson, Anne Louise, Zhu, Ying, Robinson, Bruce G., Benn, Diana E., Clifton-Bligh, Roderick J.

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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 von Marsh, Debbie J., Robinson, Bruce G., Andrew, Scott, Richardson, Anne-Louise, Pojer, Ruth, Schnitzler, Margaret, Mulligan, Lois M., Hyland, Valentine J.

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Male breast cancer in Cowden syndrome patients with germline PTEN mutations von FACKENTHAL, James D, MARSH, Deborah J, RICHARDSON, Anne-Louise, CUMMINGS, Shelly A, ENG, Charis, ROBINSON, Bruce G, OLOPADE, Olufunmilayo I

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Allelic imbalance, including deletion of PTEN/MMAC1, at the Cowden disease locus on 10q22-23, in hamartomas from patients with cowden syndrome and germline PTEN mutation von Marsh, Debbie J., Dahia, Patricia L. M., Coulon, Valérie, Zheng, Zimu, Dorion-Bonnet, Françoise, Call, Katherine M., Little, Randall, Lin, Albert Y., Eeles, Rosalind A., Goldstein, Alisa M., Hodgson, Shirley V., Richardson, Anne-Louise, Robinson, Bruce G., Weber, H. Christian, Longy, Michel, Eng, Charis

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Sporadic and familial pheochromocytomas are associated with loss of at least two discrete intervals on chromosome 1p von BENN, Diana E, DWIGHT, Trisha, RICHARDSON, Anne Louise, DELBRIDGE, Leigh, BAMBACH, Christopher P, STOWASSER, Michael, GORDON, Richard D, MARSH, Deborah J, ROBINSON, Bruce G

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Independent Genetic Events Associated with the Development of Multiple Parathyroid Tumors in Patients with Primary Hyperparathyroidism von Dwight, Trisha, Nelson, Anne E., Theodosopoulos, George, Richardson, Anne Louise, Learoyd, Diana L., Philips, Jeanette, Delbridge, Leigh, Zedenius, Jan, Teh, Bin T., Larsson, Catharina, Marsh, Deborah J., Robinson, Bruce G.

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Allelic imbalance, including deletion of PTEN/MMACI, at the Cowden disease locus on 10q22-23, in hamartomas from patients with Cowden syndrome and germline PTEN mutation von Marsh, D J, Dahia, P L, Coulon, V, Zheng, Z, Dorion-Bonnet, F, Call, K M, Little, R, Lin, A Y, Eeles, R A, Goldstein, A M, Hodgson, S V, Richardson, A L, Robinson, B G, Weber, H C, Longy, M, Eng, C

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Loss of heterozygosity in sporadic parathyroid tumours: involvement of chromosome 1 and the MEN1 gene locus in 11q13 von Dwight, Trisha, Twigg, Stephen, Delbridge, Leigh, Wong, Fung-Ki, Farnebo, Filip, Richardson, Anne Louise, Nelson, Anne, Zedenius, Jan, Philips, Jeanette, Larsson, Catharina, Teh, Bin Tean, Robinson, Bruce

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Male breast cancer in Cowden syndrome patients with germlinePTEN mutations von Fackenthal, James D, Marsh, Deborah J, Richardson, Anne-Louise, Cummings, Shelly A, Eng, Charis, Robinson, Bruce G, Olopade, Olufunmilayo I

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