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Journal of Medical Genetics|April 1, 1987
A previously undescribed syndrome of thoracic dysplasia and communicating hydrocephalus in two sibs, one diagnosed prenatally by ultrasoundR M Winter, S Campbell, J S Wigglesworth, et al.Clinical Genetics|December 1, 1981
Intrafamilial correlation in Friedreich's ataxiaR M Winter, A E Harding, M Baraitser, et al.Journal of Medical Genetics|February 25, 1998
Familial persistent pulmonary hypertension of the newborn resulting from misalignment of the pulmonary vessels (congenital alveolar capillary dysplasia)H B Vassal, M Malone, A J Petros, et al.American Journal of Human Genetics|October 1, 1992
Pelizaeus-Merzbacher disease: detection of mutations Thr181----Pro and Leu223----Pro in the proteolipid protein gene, and prenatal diagnosisS Strautnieks, P Rutland, R M Winter, et al.Clinical Dysmorphology|May 8, 1998
Rapadilino syndrome--a non-Finnish caseS G Kant, M Baraitser, P J Milla, et al.British Journal of Obstetrics and Gynaecology|August 1, 1984
The radiology of stillbirths and neonatal deathsR M Winter, B M Sandin, R A Mitchell, et al.Clinical Dysmorphology|May 13, 1999
A new syndrome of spondyloepimetaphyseal dysplasia, eczema and hypogammaglobulinaemiaS F Slaney, C M Hall, D J Atherton, et al.Clinical Dysmorphology|October 29, 2002
Dysplastic cortical hyperostosis (Kozlowski-Tsuruta syndrome): report of a second caseMohnish Suri, C Garrett, R M Winter, et al.Journal of Medical Genetics|October 1, 1992
The mapping of a gene for craniosynostosis: evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome 7pL A Brueton, L van Herwerden, K A Chotai, et al.Journal of Medical Genetics|June 1, 1990
The Baller-Gerold syndrome: phenotypic and cytogenetic overlap with Roberts syndromeS M Huson, C S Rodgers, C M Hall, et al.Pageof 19