Marsh DJ - Search Results

1

Balanced translocation of 10q and13q, including the PTEN gene, in a boy with a human chorionic gonadotropin-secreting tumor and the Bannayan-Riley-Ruvalcaba syndrome.

Faisal Ahmed S, Marsh DJ, Weremowicz S, Morton CC, Williams DM, Eng C. Faisal Ahmed S, et al. Among authors: marsh dj. J Clin Endocrinol Metab. 1999 Dec;84(12):4665-70. doi: 10.1210/jcem.84.12.6178. J Clin Endocrinol Metab. 1999. PMID: 10599735 No abstract available.

2

Absence of germline mutations in MINPP1, a phosphatase encoding gene centromeric of PTEN, in patients with Cowden and Bannayan-Riley-Ruvalcaba syndrome without germline PTEN mutations.

Dahia PM, Gimm O, Chi H, Marsh DJ, Reynolds PR, Eng C. Dahia PM, et al. Among authors: marsh dj. J Med Genet. 2000 Sep;37(9):715-7. doi: 10.1136/jmg.37.9.715. J Med Genet. 2000. PMID: 11182934 Free PMC article. No abstract available.

3

Analysis of the PTEN gene in human meningiomas.

Peters N, Wellenreuther R, Rollbrocker B, Hayashi Y, Meyer-Puttlitz B, Duerr EM, Lenartz D, Marsh DJ, Schramm J, Wiestler OD, Parsons R, Eng C, von Deimling A. Peters N, et al. Among authors: marsh dj. Neuropathol Appl Neurobiol. 1998 Feb;24(1):3-8. doi: 10.1046/j.1365-2990.1998.00093.x. Neuropathol Appl Neurobiol. 1998. PMID: 9549723

4

Germline mutations in PTEN are present in Bannayan-Zonana syndrome.

Marsh DJ, Dahia PL, Zheng Z, Liaw D, Parsons R, Gorlin RJ, Eng C. Marsh DJ, et al. Nat Genet. 1997 Aug;16(4):333-4. doi: 10.1038/ng0897-333. Nat Genet. 1997. PMID: 9241266 No abstract available.

5

Germline PTEN mutation in a family with Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome.

Zori RT, Marsh DJ, Graham GE, Marliss EB, Eng C. Zori RT, et al. Among authors: marsh dj. Am J Med Genet. 1998 Dec 4;80(4):399-402. Am J Med Genet. 1998. PMID: 9856571

6

PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.

Marsh DJ, Kum JB, Lunetta KL, Bennett MJ, Gorlin RJ, Ahmed SF, Bodurtha J, Crowe C, Curtis MA, Dasouki M, Dunn T, Feit H, Geraghty MT, Graham JM Jr, Hodgson SV, Hunter A, Korf BR, Manchester D, Miesfeldt S, Murday VA, Nathanson KL, Parisi M, Pober B, Romano C, Eng C, et al. Marsh DJ, et al. Hum Mol Genet. 1999 Aug;8(8):1461-72. doi: 10.1093/hmg/8.8.1461. Hum Mol Genet. 1999. PMID: 10400993

7

Long-chain L 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency does not appear to be the primary cause of lipid myopathy in patients with Bannayan-Riley-Ruvalcaba syndrome (BRRS).

Otto LR, Boriack RL, Marsh DJ, Kum JB, Eng C, Burlina AB, Bennett MJ. Otto LR, et al. Among authors: marsh dj. Am J Med Genet. 1999 Mar 5;83(1):3-5. doi: 10.1002/(sici)1096-8628(19990305)83:1<3::aid-ajmg2>3.0.co;2-k. Am J Med Genet. 1999. PMID: 10076877

8

Germline PTEN mutations in Cowden syndrome-like families.

Marsh DJ, Dahia PL, Caron S, Kum JB, Frayling IM, Tomlinson IP, Hughes KS, Eeles RA, Hodgson SV, Murday VA, Houlston R, Eng C. Marsh DJ, et al. J Med Genet. 1998 Nov;35(11):881-5. doi: 10.1136/jmg.35.11.881. J Med Genet. 1998. PMID: 9832031 Free PMC article.

9

Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation.

Marsh DJ, Coulon V, Lunetta KL, Rocca-Serra P, Dahia PL, Zheng Z, Liaw D, Caron S, Duboué B, Lin AY, Richardson AL, Bonnetblanc JM, Bressieux JM, Cabarrot-Moreau A, Chompret A, Demange L, Eeles RA, Yahanda AM, Fearon ER, Fricker JP, Gorlin RJ, Hodgson SV, Huson S, Lacombe D, Eng C, et al. Marsh DJ, et al. Hum Mol Genet. 1998 Mar;7(3):507-15. doi: 10.1093/hmg/7.3.507. Hum Mol Genet. 1998. PMID: 9467011

10

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome.

Liaw D, Marsh DJ, Li J, Dahia PL, Wang SI, Zheng Z, Bose S, Call KM, Tsou HC, Peacocke M, Eng C, Parsons R. Liaw D, et al. Among authors: marsh dj. Nat Genet. 1997 May;16(1):64-7. doi: 10.1038/ng0597-64. Nat Genet. 1997. PMID: 9140396

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