Suri M - Search Results

1

MURCS association with encephalocele: report of a second case.

Suri M, Brueton LA, Venkatraman N, Cox PM. Suri M, et al. Clin Dysmorphol. 2000 Jan;9(1):31-3. doi: 10.1097/00019605-200009010-00006. Clin Dysmorphol. 2000. PMID: 10649794 Review.

2

Dysplastic cortical hyperostosis (Kozlowski-Tsuruta syndrome): report of a second case.

Suri M, Garrett C, Winter RM, Hall CM, Griffiths M. Suri M, et al. Clin Dysmorphol. 2002 Oct;11(4):267-70. doi: 10.1097/00019605-200210000-00007. Clin Dysmorphol. 2002. PMID: 12401992

3

Congenital cardiac disease as a core feature of cranio-osteoarthropathy.

O'Connell S, Suri M, Duff D, Kelleher J, Hall CM, Reardon W. O'Connell S, et al. Among authors: suri m. Clin Dysmorphol. 2004 Oct;13(4):213-219. Clin Dysmorphol. 2004. PMID: 15365456

4

Relatively mild phenotype in a patient with interstitial 6q24.3-q25.2 deletion.

Tanteles GA, Yates K, Martin K, Suri M. Tanteles GA, et al. Among authors: suri m. Clin Dysmorphol. 2007 Apr;16(2):101-104. doi: 10.1097/MCD.0b013e32806e0931. Clin Dysmorphol. 2007. PMID: 17351353

5

Griscelli syndrome type 1: a report of two cases and review of the literature.

Thomas ER, Walker LJ, Pullaperuma S, Cooper B, Brueton LA, Basile GS, Suri M, Brady AF. Thomas ER, et al. Among authors: suri m. Clin Dysmorphol. 2009 Jul;18(3):145-148. doi: 10.1097/MCD.0b013e328317b870. Clin Dysmorphol. 2009. PMID: 19318926 No abstract available.

6

Mild phenotype in a patient with a de-novo 2.9-Mb interstitial deletion at 13q12.11.

Tanteles GA, Dixit A, Smith N, Martin K, Suri M. Tanteles GA, et al. Among authors: suri m. Clin Dysmorphol. 2011 Apr;20(2):61-65. doi: 10.1097/MCD.0b013e3283448498. Clin Dysmorphol. 2011. PMID: 21383552 No abstract available.

7

Denys-Drash syndrome and gonadoblastoma in a patient with Klinefelter syndrome.

Tanteles GA, Oakley S, Christian M, O'Neill D, Suri M. Tanteles GA, et al. Among authors: suri m. Clin Dysmorphol. 2011 Jul;20(3):131-135. doi: 10.1097/MCD.0b013e328346f6dc. Clin Dysmorphol. 2011. PMID: 21552011 No abstract available.

8

Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height.

Tatton-Brown K, Hanks S, Ruark E, Zachariou A, Duarte Sdel V, Ramsay E, Snape K, Murray A, Perdeaux ER, Seal S, Loveday C, Banka S, Clericuzio C, Flinter F, Magee A, McConnell V, Patton M, Raith W, Rankin J, Splitt M, Strenger V, Taylor C, Wheeler P, Temple KI, Cole T; Childhood Overgrowth Collaboration; Douglas J, Rahman N. Tatton-Brown K, et al. Oncotarget. 2011 Dec;2(12):1127-33. doi: 10.18632/oncotarget.385. Oncotarget. 2011. PMID: 22190405 Free PMC article.

9

Hypertelorism, radial ray defects, dextrocardia, hypoplastic ribs and renal anomaly: report of a second case and confirmation of the phenotype.

Fuchs GE, Suri M, Dux A, Craft EV, Vasudevan PC, Tanteles GA. Fuchs GE, et al. Among authors: suri m. Clin Dysmorphol. 2012 Jul;21(3):157-161. doi: 10.1097/MCD.0b013e328354e8cc. Clin Dysmorphol. 2012. PMID: 22610273 No abstract available.

10

Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype.

Tatton-Brown K, Murray A, Hanks S, Douglas J, Armstrong R, Banka S, Bird LM, Clericuzio CL, Cormier-Daire V, Cushing T, Flinter F, Jacquemont ML, Joss S, Kinning E, Lynch SA, Magee A, McConnell V, Medeira A, Ozono K, Patton M, Rankin J, Shears D, Simon M, Splitt M, Strenger V, Stuurman K, Taylor C, Titheradge H, Van Maldergem L, Temple IK, Cole T, Seal S; Childhood Overgrowth Consortium; Rahman N. Tatton-Brown K, et al. Am J Med Genet A. 2013 Dec;161A(12):2972-80. doi: 10.1002/ajmg.a.36229. Epub 2013 Nov 8. Am J Med Genet A. 2013. PMID: 24214728 Free article.

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