Sutcliffe MJ - Search Results

1

Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia.

Heerema NA, Raimondi SC, Anderson JR, Biegel J, Camitta BM, Cooley LD, Gaynon PS, Hirsch B, Magenis RE, McGavran L, Patil S, Pettenati MJ, Pullen J, Rao K, Roulston D, Schneider NR, Shuster JJ, Sanger W, Sutcliffe MJ, van Tuinen P, Watson MS, Carroll AJ. Heerema NA, et al. Among authors: sutcliffe mj. Genes Chromosomes Cancer. 2007 Jul;46(7):684-93. doi: 10.1002/gcc.20451. Genes Chromosomes Cancer. 2007. PMID: 17431878 Free article.

2

High concordance from independent studies by the Children's Cancer Group (CCG) and Pediatric Oncology Group (POG) associating favorable prognosis with combined trisomies 4, 10, and 17 in children with NCI Standard-Risk B-precursor Acute Lymphoblastic Leukemia: a Children's Oncology Group (COG) initiative.

Sutcliffe MJ, Shuster JJ, Sather HN, Camitta BM, Pullen J, Schultz KR, Borowitz MJ, Gaynon PS, Carroll AJ, Heerema NA. Sutcliffe MJ, et al. Leukemia. 2005 May;19(5):734-40. doi: 10.1038/sj.leu.2403673. Leukemia. 2005. PMID: 15789069

3

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

4

Hepatosplenic gamma/delta T-cell lymphoma with isochromosome 7q, translocation t(7;21), and tetrasomy 8 in a 9-year-old girl.

Rossbach HC, Chamizo W, Dumont DP, Barbosa JL, Sutcliffe MJ. Rossbach HC, et al. Among authors: sutcliffe mj. J Pediatr Hematol Oncol. 2002 Feb;24(2):154-7. doi: 10.1097/00043426-200202000-00020. J Pediatr Hematol Oncol. 2002. PMID: 11990705 Review.

5

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

6

Recipient T-cell immune reconstitution in X-linked SCID after haploidentical maternal bone marrow transplant.

de la Morena MT, Wayne AS, Day NK, Haag MM, Hinds-Frey KR, Nelson RP, Sutcliffe MJ, Good RA. de la Morena MT, et al. Among authors: sutcliffe mj. Ann N Y Acad Sci. 1995 Dec 29;770:376-7. doi: 10.1111/j.1749-6632.1995.tb31074.x. Ann N Y Acad Sci. 1995. PMID: 8597380 No abstract available.

7

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

8

Composite adrenal anaplastic neuroblastoma and virilizing adrenocortical tumor with germline TP53 R248W mutation.

Rossbach HC, Baschinsky D, Wynn T, Obzut D, Sutcliffe M, Tebbi C. Rossbach HC, et al. Pediatr Blood Cancer. 2008 Mar;50(3):681-3. doi: 10.1002/pbc.21219. Pediatr Blood Cancer. 2008. PMID: 17427234

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

Monosomy 6q1: syndrome delineation.

Romie SS, Hartsfield JK Jr, Sutcliffe MJ, Dumont DP, Kousseff BG. Romie SS, et al. Among authors: sutcliffe mj. Am J Med Genet. 1996 Mar 15;62(2):105-8. doi: 10.1002/(SICI)1096-8628(19960315)62:2<105::AID-AJMG1>3.0.CO;2-V. Am J Med Genet. 1996. PMID: 8882389

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