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Journal of Medical Genetics|June 1, 1989
Microcephaly, mental retardation, cataracts, and hypogonadism in sibs: Martsolf's syndromeM G Harbord, M Baraitser, J WilsonAmerican Journal of Medical Genetics|September 15, 1991
Autosomal dominant transmission of congenital erythroid hypoplastic anemia with radial abnormalitiesJ A Hurst, M Baraitser, B WonkeJournal of Medical Genetics|September 1, 1995
Detection of hemizygosity at the elastin locus by FISH analysis as a diagnostic test in both classical and atypical cases of Williams syndromeI Borg, J D Delhanty, M BaraitserBritish Medical Journal|June 25, 1977
Persistent measles infection in malnourished childrenJ Dossetor, H C Whittle, B M GreenwoodAmerican Journal of Medical Genetics|January 1, 1988
Distinctive syndrome of short stature, craniosynostosis, skeletal changes, and malformed earsJ A Hurst, R M Winter, M BaraitserClinical Dysmorphology|October 1, 1996
A distinctive overgrowth syndrome with polysyndactylyA Barnicoat, M Salman, L Chitty, et al.Journal of Medical Genetics|July 1, 1989
Severe Silver-Russell syndromeD Donnai, E Thompson, J Allanson, et al.Journal of Medical Genetics|December 1, 1988
Congenital spinal deformity in a three generation familyI K Temple, T G Thomas, M BaraitserJournal of Medical Genetics|August 1, 1980
Pitfalls of genetic counselling in Pfeiffer's syndromeM Baraitser, M Bowen-Bravery, P Saldaña-GarciaJournal of Neurology, Neurosurgery, and Psychiatry|June 1, 1980
Peripheral and central somatosensory nerve conduction defects in Friedreich's ataxiaS J Jones, M Baraitser, A M HallidayPageof 417