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Clinical Genetics|December 1, 1981
Intrafamilial correlation in Friedreich's ataxiaR M Winter, A E Harding, M Baraitser, et al.Journal of Medical Genetics|January 1, 1988
Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndromeM Baraitser, R M WinterJournal of Medical Genetics|January 1, 1988
A recognisable short stature syndrome with premature aging and pigmented naeviM Baraitser, J Insley, R M WinterMovement Disorders : Official Journal of the Movement Disorder Society|January 1, 1988
Genetic prediction in Huntington's disease: what are the limitations imposed by pedigree structure?V P Misra, M Baraitser, A E HardingAmerican Journal of Medical Genetics|January 1, 1988
Distinctive syndrome of short stature, craniosynostosis, skeletal changes, and malformed earsJ A Hurst, R M Winter, M BaraitserJournal of Medical Genetics|April 1, 1984
A computerised data base for the diagnosis of rare dysmorphic syndromesR M Winter, M Baraitser, J M DouglasClinical Dysmorphology|October 1, 1993
Kivlin syndrome and Peters'-Plus syndrome: are they the same disorder?E M Thompson, R M Winter, M BaraitserClinical Genetics|October 1, 1983
Greig cephalopolysyndactyly: report of 13 affected individuals in three familiesM Baraitser, R M Winter, E M BrettAmerican Journal of Medical Genetics|December 1, 1987
A syndrome of mental retardation, short stature, hemolytic anemia, delayed puberty, and abnormal facial appearance: similarities to a report of aldolase A deficiencyJ A Hurst, M Baraitser, R M WinterJournal of Medical Genetics|March 1, 1992
Distal spinal muscular atrophy with vocal cord paralysisC Pridmore, M Baraitser, E M Brett, et al.Pageof 49