Callen DF - Search Results

1

Origins of accessory small ring marker chromosomes derived from chromosome 1.

Callen DF, Eyre H, Fang YY, Guan XY, Veleba A, Martin NJ, McGill J, Haan EA. Callen DF, et al. J Med Genet. 1999 Nov;36(11):847-53. J Med Genet. 1999. PMID: 10544230 Free PMC article.

2

A rare heteromorphism of chromosome 20 and reproductive loss.

Romain DR, Whyte S, Callen DF, Eyre HJ. Romain DR, et al. Among authors: callen df. J Med Genet. 1991 Jul;28(7):477-8. doi: 10.1136/jmg.28.7.477. J Med Genet. 1991. PMID: 1895318 Free PMC article.

3

Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics.

Callen DF, Eyre HJ, Ringenbergs ML, Freemantle CJ, Woodroffe P, Haan EA. Callen DF, et al. Am J Hum Genet. 1991 Apr;48(4):769-82. Am J Hum Genet. 1991. PMID: 2014800 Free PMC article.

4

A dicentric variant of chromosome 6: characterization by use of in situ hybridisation with the biotinylated probe p308.

Callen DF, Eyre HJ, Ringenbergs ML. Callen DF, et al. Clin Genet. 1990 Feb;37(2):81-3. doi: 10.1111/j.1399-0004.1990.tb03483.x. Clin Genet. 1990. PMID: 2311270

5

Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16.

Callen DF, Ringenbergs ML, Fowler JC, Freemantle CJ, Haan EA. Callen DF, et al. J Med Genet. 1990 Mar;27(3):155-9. doi: 10.1136/jmg.27.3.155. J Med Genet. 1990. PMID: 2325088 Free PMC article.

6

The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization.

Callen DF, Freemantle CJ, Ringenbergs ML, Baker E, Eyre HJ, Romain D, Haan EA. Callen DF, et al. Am J Hum Genet. 1990 Sep;47(3):493-8. Am J Hum Genet. 1990. PMID: 2393023 Free PMC article.

7

Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q.

Haan EA, Hull YJ, White S, Cockington R, Charlton P, Callen DF. Haan EA, et al. Among authors: callen df. Am J Med Genet. 1989 Apr;32(4):490-4. doi: 10.1002/ajmg.1320320412. Am J Med Genet. 1989. PMID: 2773990

8

Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4.

Fang YY, Eyre HJ, Bohlander SK, Estop A, McPherson E, Träger T, Riess O, Callen DF. Fang YY, et al. Among authors: callen df. Am J Hum Genet. 1995 Nov;57(5):1137-42. Am J Hum Genet. 1995. PMID: 7485165 Free PMC article.

9

Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivation.

Callen DF, Eyre HJ, Dolman G, Garry-Battersby MB, McCreanor JR, Valeba A, McGill JJ. Callen DF, et al. J Med Genet. 1995 Feb;32(2):113-6. doi: 10.1136/jmg.32.2.113. J Med Genet. 1995. PMID: 7760319 Free PMC article.

10

High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype.

Callen DF, Eyre H, Lane S, Shen Y, Hansmann I, Spinner N, Zackai E, McDonald-McGinn D, Schuffenhauer S, Wauters J, et al. Callen DF, et al. J Med Genet. 1993 Oct;30(10):828-32. doi: 10.1136/jmg.30.10.828. J Med Genet. 1993. PMID: 8230159 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

261 results

Search Page

Filters