Dennis NR - Search Results

1

The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes.

Gribble SM, Prigmore E, Burford DC, Porter KM, Ng BL, Douglas EJ, Fiegler H, Carr P, Kalaitzopoulos D, Clegg S, Sandstrom R, Temple IK, Youings SA, Thomas NS, Dennis NR, Jacobs PA, Crolla JA, Carter NP. Gribble SM, et al. Among authors: dennis nr. J Med Genet. 2005 Jan;42(1):8-16. doi: 10.1136/jmg.2004.024141. J Med Genet. 2005. PMID: 15635069 Free PMC article.

2

Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays.

Fiegler H, Gribble SM, Burford DC, Carr P, Prigmore E, Porter KM, Clegg S, Crolla JA, Dennis NR, Jacobs P, Carter NP. Fiegler H, et al. Among authors: dennis nr. J Med Genet. 2003 Sep;40(9):664-70. doi: 10.1136/jmg.40.9.664. J Med Genet. 2003. PMID: 12960211 Free PMC article.

3

A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man.

Crolla JA, Dennis NR, Jacobs PA. Crolla JA, et al. Among authors: dennis nr. J Med Genet. 1992 Oct;29(10):699-703. doi: 10.1136/jmg.29.10.699. J Med Genet. 1992. PMID: 1433228 Free PMC article.

4

Parental and chromosomal origin of unbalanced de novo structural chromosome abnormalities in man.

Thomas NS, Durkie M, Van Zyl B, Sanford R, Potts G, Youings S, Dennis N, Jacobs P. Thomas NS, et al. Hum Genet. 2006 May;119(4):444-50. doi: 10.1007/s00439-006-0157-6. Epub 2006 Feb 22. Hum Genet. 2006. PMID: 16493556

5

A familial balanced inverted insertion ins(15)(q15q13q11.2) producing Prader-Willi syndrome, Angelman syndrome and duplication of 15q11.2-q13 in a single family: Importance of differentiation from a paracentric inversion.

Collinson MN, Roberts SE, Crolla JA, Dennis NR. Collinson MN, et al. Among authors: dennis nr. Am J Med Genet A. 2004 Apr 1;126A(1):27-32. doi: 10.1002/ajmg.a.26565. Am J Med Genet A. 2004. PMID: 15039970

6

A comparison of the clinical and cytogenetic findings in nine patients with a ring (X) cell line and 16 45,X patients.

Collins AL, Cockwell AE, Jacobs PA, Dennis NR. Collins AL, et al. Among authors: dennis nr. J Med Genet. 1994 Jul;31(7):528-33. doi: 10.1136/jmg.31.7.528. J Med Genet. 1994. PMID: 7966189 Free PMC article. Review.

7

Three patients with ring (X) chromosomes and a severe phenotype.

Dennis NR, Collins AL, Crolla JA, Cockwell AE, Fisher AM, Jacobs PA. Dennis NR, et al. J Med Genet. 1993 Jun;30(6):482-6. doi: 10.1136/jmg.30.6.482. J Med Genet. 1993. PMID: 8326492 Free PMC article.

8

Unbalanced translocation in a mother and her son in one of two 5;10 translocation families.

Barber JC, Temple IK, Campbell PL, Collinson MN, Campbell CM, Renshaw RM, Dennis NR. Barber JC, et al. Among authors: dennis nr. Am J Med Genet. 1996 Mar 1;62(1):84-90. doi: 10.1002/(SICI)1096-8628(19960301)62:1<84::AID-AJMG17>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8779332

9

A molecular and FISH approach to determining karyotype and phenotype correlations in six patients with supernumerary marker(22) chromosomes.

Crolla JA, Howard P, Mitchell C, Long FL, Dennis NR. Crolla JA, et al. Among authors: dennis nr. Am J Med Genet. 1997 Nov 12;72(4):440-7. doi: 10.1002/(sici)1096-8628(19971112)72:4<440::aid-ajmg13>3.0.co;2-r. Am J Med Genet. 1997. PMID: 9375728

10

FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosomes 15 and 22: I. Results of 26 new cases.

Crolla JA, Long F, Rivera H, Dennis NR. Crolla JA, et al. Among authors: dennis nr. Am J Med Genet. 1998 Feb 3;75(4):355-66. doi: 10.1002/(sici)1096-8628(19980203)75:4<355::aid-ajmg4>3.0.co;2-p. Am J Med Genet. 1998. PMID: 9482641

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