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Journal of Medical Genetics|February 1, 1988
Norrie disease resulting from a gene deletion: clinical features and DNA studiesD Donnai, R C Mountford, A P ReadAmerican Journal of Medical Genetics|February 15, 1992
Monozygotic twinning and Wiedemann-Beckwith syndromeJ Clayton-Smith, A P Read, D DonnaiBritish Journal of Obstetrics and Gynaecology|May 1, 1980
Comparison of pregnancy outcome after amniocentesis for previous neural tube defect or raised maternal serum alphafetoproteinA P Read, D Donnai, R Harris, et al.Journal of Medical Genetics|December 1, 1988
Hypomelanosis of Ito: a manifestation of mosaicism or chimerismD Donnai, A P Read, C McKeown, et al.British Journal of Obstetrics and Gynaecology|February 1, 1982
Amniotic fluid acetylcholinesterase: a retrospective and prospective study of the qualitative methodA P Read, S J Fennell, D Donnai, et al.Clinical Dysmorphology|January 1, 1992
Fetus with unbalanced translocation involving chromosomes 2 and 11A M Norman, A P Read, A Clark, et al.European Journal of Human Genetics : EJHG|May 30, 2003
Mutations in PAX1 may be associated with Klippel-Feil syndromeJ M McGaughran, A Oates, D Donnai, et al.European Journal of Human Genetics : EJHG|November 26, 1999
A transcription factor involved in skeletal muscle gene expression is deleted in patients with Williams syndromeM Tassabehji, M Carette, C Wilmot, et al.American Journal of Medical Genetics|February 15, 1992
Recurrent Wiedemann-Beckwith syndrome with inversion of chromosome (11)(p11.2p15.5)A M Norman, A P Read, J Clayton-Smith, et al.American Journal of Human Genetics|July 1, 1991
The gene for Treacher Collins syndrome maps to the long arm of chromosome 5M J Dixon, A P Read, D Donnai, et al.Pageof 19