Sutcliffe MJ - Search Results

1

Translocation breakpoint in two unrelated Tourette syndrome cases, within a region previously linked to the disorder.

Crawford FC, Ait-Ghezala G, Morris M, Sutcliffe MJ, Hauser RA, Silver AA, Mullan MJ. Crawford FC, et al. Among authors: sutcliffe mj. Hum Genet. 2003 Jul;113(2):154-61. doi: 10.1007/s00439-003-0942-4. Epub 2003 Apr 16. Hum Genet. 2003. PMID: 12698358

2

Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adult.

Papenhausen PR, Mueller OT, Johnson VP, Sutcliffe M, Diamond TM, Kousseff BG. Papenhausen PR, et al. Am J Med Genet. 1995 Nov 20;59(3):271-5. doi: 10.1002/ajmg.1320590302. Am J Med Genet. 1995. PMID: 8599348 Review.

3

Chromosome 3p25 deletion in mother and daughter with minimal phenotypic effect.

Takagishi J, Rauen KA, Drumheller T, Kousseff B, Sutcliffe M. Takagishi J, et al. Am J Med Genet A. 2006 Jul 15;140(14):1587-93. doi: 10.1002/ajmg.a.31325. Am J Med Genet A. 2006. PMID: 16770804

4

A patient with an interstitial duplication of chromosome 5p11-p13.3 further confirming a critical region for 5p duplication syndrome.

Loscalzo ML, Becker TA, Sutcliffe M. Loscalzo ML, et al. Eur J Med Genet. 2008 Jan-Feb;51(1):54-60. doi: 10.1016/j.ejmg.2007.09.006. Epub 2007 Oct 6. Eur J Med Genet. 2008. PMID: 18006398

5

Three cell line mosaicism involving structural and numerical abnormalities of chromosome 18 in a 3.5-year-old girl: 47,XX,+18/47,XX,+del(18)(q22)/46,XX.

Sutcliffe MJ, Mueller OT, Kousseff BG, Dumont DP, McFarland JA, Mawani F, Conforto D, Ranells JD. Sutcliffe MJ, et al. Am J Med Genet. 2001 Aug 1;102(2):192-9. doi: 10.1002/1096-8628(20010801)102:2<192::aid-ajmg1445>3.0.co;2-d. Am J Med Genet. 2001. PMID: 11477615

6

Extreme variant of enlarged heterochromatin region on chromosome 9Q in a normal child and multiple family members.

Steffensen TS, Gilbert-Barness E, Sandstrom M, Bell JR, Bryan J, Sutcliffe MJ. Steffensen TS, et al. Among authors: sutcliffe mj. Fetal Pediatr Pathol. 2009;28(6):247-52. doi: 10.1080/15513810903203180. Fetal Pediatr Pathol. 2009. PMID: 19842879

7

Assignment1 of microsomal epoxide hydrolase (EPHX1) to human chromosome 1q42.1 by in situ hybridization.

Hartsfield JK Jr, Sutcliffe MJ, Everett ET, Hassett C, Omiecinski CJ, Saari JA. Hartsfield JK Jr, et al. Among authors: sutcliffe mj. Cytogenet Cell Genet. 1998;83(1-2):44-5. doi: 10.1159/000015164. Cytogenet Cell Genet. 1998. PMID: 9925921 No abstract available.

8

Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adult.

Papenhausen PR, Mueller OT, Sutcliffe M, Diamond TM, Kousseff BG, Johnson VP. Papenhausen PR, et al. Am J Med Genet. 1996 Dec 2;66(1):90. doi: 10.1002/(SICI)1096-8628(19961202)66:1<90::AID-AJMG23>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8957521 No abstract available.

9

Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome.

Rossbach HC, Sutcliffe MJ, Haag MM, Grana NH, Rossi AR, Barbosa JL. Rossbach HC, et al. Among authors: sutcliffe mj. Am J Med Genet. 1996 Jan 2;61(1):65-7. doi: 10.1002/(SICI)1096-8628(19960102)61:1<65::AID-AJMG12>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8741921

10

Pre-B acute lymphoblastic leukemia in a 3-year-old boy with pre-acute myelogenous leukemia myelodysplastic syndrome: cytogenetic evidence of common early progenitor cell ontogeny.

Rossbach HC, Sutcliffe MJ, Chamizo W, Haag MM, Grana NH, Washington KR, Barbosa JL. Rossbach HC, et al. Among authors: sutcliffe mj. J Pediatr Hematol Oncol. 1998 Jul-Aug;20(4):347-52. doi: 10.1097/00043426-199807000-00014. J Pediatr Hematol Oncol. 1998. PMID: 9703011

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