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Author/Creator Menzel, C

1. A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocation. Issue 6 (1st June 2002)

Authors:
Borg, I; Squire, M; Menzel, C; Stout, K; Morgan, D; Willatt, L; O'Brien, P C M; Ferguson-Smith, M A; Ropers, H H; Tommerup, N; Kalscheuer, V M; Sargan, D R
Journal:
Journal of medical genetics
Issue:
Volume 39:Issue 6(2002)
Page Start:
391
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes. Issue 4 (1st April 1999)

Authors:
Wirth, J; Nothwang, H-G; van der Maarel, S; Menzel, C; Borck, G; Lopez-Pajares, I; Brøndum-Nielsen, K; Tommerup, N; Bugge, M; Ropers, H-H; Haaf, T
Journal:
Journal of medical genetics
Issue:
Volume 36:Issue 4(1999)
Page Start:
271
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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