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Journal of Medical Genetics|October 1, 1994
Chimaerism shown by cytogenetics and DNA polymorphism analysisA J Green, D E Barton, P Jenks, et al.Journal of Medical Genetics|December 1, 1983
Phenotype-genotype correlation in haemoglobin H disease in childhoodR Galanello, M Pirastu, M A Melis, et al.Journal of Medical Genetics|December 1, 1981
A case of the orocraniodigital (Juberg-Hayward) syndromeN C Nevin, P Henry, P T ThomasJournal of Medical Genetics|December 1, 1982
Studies on the origin of human amniotic fluid cells by immunofluorescent staining of keratin filamentsW W ChenJournal of Medical Genetics|July 1, 1994
Paternal transmission of congenital myotonic dystrophyJ Bergoffen, J Kant, J Sladky, et al.Journal of Medical Genetics|July 1, 1994
A comparison of the clinical and cytogenetic findings in nine patients with a ring (X) cell line and 16 45,X patientsA L Collins, A E Cockwell, P A Jacobs, et al.Journal of Medical Genetics|October 1, 1976
Spinal dysraphism: genetic relation to neural tube malformationsC O Carter, K A Evans, K TillJournal of Medical Genetics|December 1, 1994
Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal familiesM Bitner-Glindzicz, Y de Kok, D Summers, et al.Journal of Medical Genetics|December 1, 1994
The impact of genetic counselling on females in fragile X familiesG Curtis, N Dennis, J MacPhersonPageof 649