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Journal of Medical Genetics|July 1, 1989
Blepharophimosis plus ovarian failure: a likely candidate for a contiguous gene syndromeA Smith, I S Fraser, R P Shearman, et al.Journal of Medical Genetics|July 1, 1989
Severe Silver-Russell syndromeD Donnai, E Thompson, J Allanson, et al.Journal of Medical Genetics|July 1, 1989
Kyphomelic dysplasiaI K Temple, E M Thompson, C M Hall, et al.Journal of Medical Genetics|July 1, 1989
Unknown syndrome: Noonan-like craniofacial features, digital anomalies, and premature birthR C Shepherd, D R Goudie, J L TolmieJournal of Medical Genetics|November 1, 1988
A progressive cone-rod dystrophy and amelogenesis imperfecta: a new syndromeI K Jalili, N J SmithJournal of Medical Genetics|December 1, 1988
Congenital spinal deformity in a three generation familyI K Temple, T G Thomas, M BaraitserJournal of Medical Genetics|December 1, 1988
Localisation of human alpha globin to 16p13.3----pterV J Buckle, D R Higgs, A O Wilkie, et al.Journal of Medical Genetics|December 1, 1988
Apparent monosomy 21 owing to a ring 21 chromosome: parental origin revealed by DNA analysisR Dalgleish, D P Duckett, M Woodhouse, et al.Journal of Medical Genetics|May 2, 2020
Uptake of pre-symptomatic testing for BRCA1 and BRCA2 is age, gender, offspring and time-dependentClaire Forde, Kate Brunstrom, Emma Woodward, et al.Journal of Medical Genetics|June 18, 2020
SETD1B-associated neurodevelopmental disorderAlexandra Roston, Dan Evans, Harinder Gill, et al.Pageof 649