Cross I - Search Results

1

Characterisation of interstitial duplications and triplications of chromosome 15q11-q13.

Roberts SE, Dennis NR, Browne CE, Willatt L, Woods G, Cross I, Jacobs PA, Thomas S. Roberts SE, et al. Among authors: cross i. Hum Genet. 2002 Mar;110(3):227-34. doi: 10.1007/s00439-002-0678-6. Epub 2002 Feb 2. Hum Genet. 2002. PMID: 11935334

2

Neurofibromatosis pseudogene amplification underlies euchromatic cytogenetic duplications and triplications of proximal 15q.

Barber JC, Cross IE, Douglas F, Nicholson JC, Moore KJ, Browne CE. Barber JC, et al. Among authors: cross ie. Hum Genet. 1998 Nov;103(5):600-7. doi: 10.1007/s004390050875. Hum Genet. 1998. PMID: 9860303

3

A prospective cytogenetic study of 36 cases of DiGeorge syndrome.

Wilson DI, Cross IE, Goodship JA, Brown J, Scambler PJ, Bain HH, Taylor JF, Walsh K, Bankier A, Burn J, et al. Wilson DI, et al. Among authors: cross ie. Am J Hum Genet. 1992 Nov;51(5):957-63. Am J Hum Genet. 1992. PMID: 1415264 Free PMC article.

4

FISH studies in a patient with sporadic aniridia and t(7;11) (q31.2;p13).

Crolla JA, Cross I, Atkey N, Wright M, Oley CA. Crolla JA, et al. Among authors: cross i. J Med Genet. 1996 Jan;33(1):66-8. doi: 10.1136/jmg.33.1.66. J Med Genet. 1996. PMID: 8825052 Free PMC article.

5

A de novo translocation t(3;17)(q26.3;q23.1) in a child with Cornelia de Lange syndrome.

Ireland M, English C, Cross I, Houlsby WT, Burn J. Ireland M, et al. Among authors: cross i. J Med Genet. 1991 Sep;28(9):639-40. doi: 10.1136/jmg.28.9.639. J Med Genet. 1991. PMID: 1956066 Free PMC article.

6

Monozygotic twins with chromosome 22q11 deletion and discordant phenotype.

Goodship J, Cross I, Scambler P, Burn J. Goodship J, et al. Among authors: cross i. J Med Genet. 1995 Sep;32(9):746-8. doi: 10.1136/jmg.32.9.746. J Med Genet. 1995. PMID: 8544199 Free PMC article.

7

Partial trisomy 20p resulting from a recombination of a familial pericentric inversion.

Bown N, Cross I, Davison EV, Burn J. Bown N, et al. Among authors: cross i. Hum Genet. 1986 Dec;74(4):417-9. doi: 10.1007/BF00280496. Hum Genet. 1986. PMID: 3793104

8

Deletions within chromosome 22q11 in familial congenital heart disease.

Wilson DI, Goodship JA, Burn J, Cross IE, Scambler PJ. Wilson DI, et al. Among authors: cross ie. Lancet. 1992 Sep 5;340(8819):573-5. doi: 10.1016/0140-6736(92)92107-q. Lancet. 1992. PMID: 1355155

9

A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation.

Goodship J, Curtis A, Cross I, Brown J, Emslie J, Wolstenholme J, Bhattacharya S, Burn J. Goodship J, et al. Among authors: cross i. J Med Genet. 1992 Jul;29(7):451-4. J Med Genet. 1992. PMID: 1640422 Free PMC article.

10

Alagille syndrome and deletion of 20p.

Anad F, Burn J, Matthews D, Cross I, Davison BC, Mueller R, Sands M, Lillington DM, Eastham E. Anad F, et al. Among authors: cross i. J Med Genet. 1990 Dec;27(12):729-37. doi: 10.1136/jmg.27.12.729. J Med Genet. 1990. PMID: 2074558 Free PMC article. Review.

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