Bryke C - Search Results

1

Clinical and molecular characterization of overlapping interstitial Xp21-p22 duplications in two unrelated individuals.

Thorson L, Bryke C, Rice G, Artzer A, Schilz C, Israel J, Huber S, Laffin J, Raca G. Thorson L, et al. Among authors: bryke c. Am J Med Genet A. 2010 Apr;152A(4):904-15. doi: 10.1002/ajmg.a.33340. Am J Med Genet A. 2010. PMID: 20358600

2

Assessing copy number abnormalities and copy-neutral loss-of-heterozygosity across the genome as best practice in diagnostic evaluation of acute myeloid leukemia: An evidence-based review from the cancer genomics consortium (CGC) myeloid neoplasms working group.

Xu X, Bryke C, Sukhanova M, Huxley E, Dash DP, Dixon-Mciver A, Fang M, Griepp PT, Hodge JC, Iqbal A, Jeffries S, Kanagal-Shamanna R, Quintero-Rivera F, Shetty S, Slovak ML, Yenamandra A, Lennon PA, Raca G. Xu X, et al. Among authors: bryke c. Cancer Genet. 2018 Dec;228-229:218-235. doi: 10.1016/j.cancergen.2018.07.005. Epub 2018 Oct 6. Cancer Genet. 2018. PMID: 30344013 Free article. Review.

3

Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasms.

Kanagal-Shamanna R, Hodge JC, Tucker T, Shetty S, Yenamandra A, Dixon-McIver A, Bryke C, Huxley E, Lennon PA, Raca G, Xu X, Jeffries S, Quintero-Rivera F, Greipp PT, Slovak ML, Iqbal MA, Fang M. Kanagal-Shamanna R, et al. Among authors: bryke c. Cancer Genet. 2018 Dec;228-229:197-217. doi: 10.1016/j.cancergen.2018.07.003. Epub 2018 Oct 10. Cancer Genet. 2018. PMID: 30377088 Free article. Review.

4

Duplication of euchromatin without phenotypic effects: a variant of chromosome 16.

Bryke CR, Breg WR, Potluri VR, Yang-Feng TL. Bryke CR, et al. Am J Med Genet. 1990 May;36(1):43-4. doi: 10.1002/ajmg.1320360110. Am J Med Genet. 1990. PMID: 2333906

5

Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes.

Lindgren V, Chen CP, Bryke CR, Lichter P, Page DC, Yang-Feng TL. Lindgren V, et al. Among authors: bryke cr. Hum Genet. 1992 Feb;88(4):393-8. doi: 10.1007/BF00215672. Hum Genet. 1992. PMID: 1740316

6

Novel isodicentric chromosome 18 in an abnormal infant with a mosaic karyotype [46,XY/46,XY,-18,+dic(18)(q12.2]).

Bryke CR, Lindgren V, Fryburg JS, Yang-Feng TL. Bryke CR, et al. Am J Med Genet. 1990 Jun;36(2):247-50. doi: 10.1002/ajmg.1320360221. Am J Med Genet. 1990. PMID: 2368814

7

Distinct missense mutations of the FGFR3 lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype.

Bellus GA, Spector EB, Speiser PW, Weaver CA, Garber AT, Bryke CR, Israel J, Rosengren SS, Webster MK, Donoghue DJ, Francomano CA. Bellus GA, et al. Among authors: bryke cr. Am J Hum Genet. 2000 Dec;67(6):1411-21. doi: 10.1086/316892. Epub 2000 Oct 27. Am J Hum Genet. 2000. PMID: 11055896 Free PMC article.

8

Phenotypic, cytogenetic, and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposis.

Lindgren V, Bryke CR, Ozcelik T, Yang-Feng TL, Francke U. Lindgren V, et al. Among authors: bryke cr. Am J Hum Genet. 1992 May;50(5):988-97. Am J Hum Genet. 1992. PMID: 1315124 Free PMC article. Review.

9

Antenatal diagnosis of 45,X/48,XYYY.

Bryke CR, Mahoney MJ, Yang-Feng TL. Bryke CR, et al. Am J Med Genet. 1989 Oct;34(2):207-10. doi: 10.1002/ajmg.1320340215. Am J Med Genet. 1989. PMID: 2816999

10

Incidence and patterns of ALK FISH abnormalities seen in a large unselected series of lung carcinomas.

Dai Z, Kelly JC, Meloni-Ehrig A, Slovak ML, Boles D, Christacos NC, Bryke CR, Schonberg SA, Otani-Rosa J, Pan Q, Ho AK, Sanders HR, Zhang ZJ, Jones D, Mowrey PN. Dai Z, et al. Among authors: bryke cr. Mol Cytogenet. 2012 Dec 3;5(1):44. doi: 10.1186/1755-8166-5-44. Mol Cytogenet. 2012. PMID: 23198868 Free PMC article.

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