Articles

	Review of `The provision of services for the prenatal diagnosis of fetal abnormality in the United Kingdom'. Report of the Clinical Genetics Society Working Party. Supplement No 3 to the Bulletin of the Eugenics Society, November 1978 John A Raeburn J Med Genet 1980; 17: 313. doi:10.1136/jmg.17.4.313 [PDF] [Request Permissions]

Correspondence

	Correspondence Elizabeth Riley and Michael Swift J Med Genet 1980; 17: 324. doi:10.1136/jmg.17.4.324-a [PDF] [Request Permissions]
	Correspondence N. Fitch J Med Genet 1980; 17: 325. doi:10.1136/jmg.17.4.325 [PDF] [Request Permissions]
	Correspondence Alan R Rushton and Bennett A Shaywitz J Med Genet 1980; 17: 326. doi:10.1136/jmg.17.4.326 [PDF] [Request Permissions]
	Correspondence W A Campbell and W H Price J Med Genet 1980; 17: 327. doi:10.1136/jmg.17.4.327 [PDF] [Request Permissions]

Articles

	Review of `The provision of services for the prenatal diagnosis of fetal abnormality in the United Kingdom'. Report of the Clinical Genetics Society Working Party. Supplement No 3 to the Bulletin of the Eugenics Society, November 1978 John A Raeburn J Med Genet 1980; 17: 313. doi:10.1136/jmg.17.4.313 [PDF] [Request Permissions]

Research Article

	Incidence of Duchenne muscular dystrophy in New South Wales and Australian Capital Territory. J Cowan, J Macdessi, A Stark, and G Morgan J Med Genet 1980; 17: 245-249. doi:10.1136/jmg.17.4.245 [Abstract] [PDF] [Request Permissions]
	Pitfalls of genetic counselling in Pfeiffer's syndrome. M Baraitser, M Bowen-Bravery, and P Saldaña-Garcia J Med Genet 1980; 17: 250-256. doi:10.1136/jmg.17.4.250 [Abstract] [PDF] [Request Permissions]
	Menkes X linked disease: heterozygous phenotype in uncloned fibroblast cultures. N Horn J Med Genet 1980; 17: 257-261. doi:10.1136/jmg.17.4.257 [Abstract] [PDF] [Request Permissions]
	Menkes X linked disease: two clonal cell populations in heterozygotes. N Horn, P Mooy, and V M McGuire J Med Genet 1980; 17: 262-266. doi:10.1136/jmg.17.4.262 [Abstract] [PDF] [Request Permissions]
	Increase in the amount of fetal lymphocytes in maternal blood during pregnancy. E L Assche and C Susanne J Med Genet 1980; 17: 267-272. doi:10.1136/jmg.17.4.267 [Abstract] [PDF] [Request Permissions]
	Estimates of the likelihood that a Down's syndrome child of unknown genotype is a consequence of an inherited translocation. S G Albright and E B Hook J Med Genet 1980; 17: 273-276. doi:10.1136/jmg.17.4.273 [Abstract] [PDF] [Request Permissions]
	A family with diaphyseal aclasis and peripheral dysostosis. A P Brooks and R Wynne-Davies J Med Genet 1980; 17: 277-280. doi:10.1136/jmg.17.4.277 [Abstract] [PDF] [Request Permissions]
	Negro alpha-thalassaemia: genetic studies in homozygous sickle cell disease. G R Serjeant, K P Mason, and B E Serjeant J Med Genet 1980; 17: 281-284. doi:10.1136/jmg.17.4.281 [Abstract] [PDF] [Request Permissions]
	Haemoglobin E trait and probable alpha-thalassaemia in a black American family: a family study. A F El-Shirbiny, S Parkhurst, R E Bettigole, and K D Tourbaf J Med Genet 1980; 17: 285-287. doi:10.1136/jmg.17.4.285 [Abstract] [PDF] [Request Permissions]
	Recessively inherited growth hormone deficiency in a family from Iraq. M D Donaldson, S M Tucker, and D B Grant J Med Genet 1980; 17: 288-290. doi:10.1136/jmg.17.4.288 [Abstract] [PDF] [Request Permissions]
	Female phenotype and multiple abnormalities in sibs with a Y chromosome and partial X chromosome duplication: H--Y antigen and Xg blood group findings. R Bernstein, T Jenkins, B Dawson, J Wagner, G Dewald, G C Koo, and S S Wachtel J Med Genet 1980; 17: 291-300. doi:10.1136/jmg.17.4.291 [Abstract] [PDF] [Request Permissions]
	Dermatoglyphs in carriers of a balanced 15;21 translocation. A Rodewald, M Zankl, H Zankl, and K D Zang J Med Genet 1980; 17: 301-305. doi:10.1136/jmg.17.4.301 [Abstract] [PDF] [Request Permissions]
	Segregation of an X ring chromosome in two generations. B Dallapiccola, L Bruni, B Boscherini, A M Pasquino, L Chessa, and P Vignetti J Med Genet 1980; 17: 306-308. doi:10.1136/jmg.17.4.306 [Abstract] [PDF] [Request Permissions]
	Pericentric inversion (13) with two different recombinants in the same family. E M Williamson, J F Miller, and M Seabright J Med Genet 1980; 17: 309-312. doi:10.1136/jmg.17.4.309 [Abstract] [PDF] [Request Permissions]
	Prenatal diagnosis of a de novo non-fluorescent Y chromosome. J H Priest, A T Chen, P M Fernhoff, J A Reidy, and C Whitsett J Med Genet 1980; 17: 314-316. doi:10.1136/jmg.17.4.314 [Abstract] [PDF] [Request Permissions]
	13q-/r(13) mosaicism. N Niikawa, T Tamura, F Tomiyasu, and T Kajii J Med Genet 1980; 17: 316-319. doi:10.1136/jmg.17.4.316 [Abstract] [PDF] [Request Permissions]
	45,X/46,XY/47,XY, +21 mosaicism in a hypogonadal phenotypic male. M Sparagana, P W Wong, T R Dorsch, C Casten, M Rauer, and K Szego J Med Genet 1980; 17: 319-321. doi:10.1136/jmg.17.4.319 [Abstract] [PDF] [Request Permissions]
	Gonadal dysgenesis in a 46,XY female mosaic for double autosomal trisomies 8 and 21. J M Sulewski, Thao-phuong-Dang, S Ward, and R L Ladda J Med Genet 1980; 17: 321-323. doi:10.1136/jmg.17.4.321 [Abstract] [PDF] [Request Permissions]
	Congenital horizontal gaze palsy and kyphoscoliosis. E K Dretakis J Med Genet 1980; 17: 324. doi:10.1136/jmg.17.4.324 [PDF] [Request Permissions]
	Classification of inherited brachydactylies. H K Goswami and B D Chaurasia J Med Genet 1980; 17: 324-325. doi:10.1136/jmg.17.4.324-b [PDF] [Request Permissions]
	Autosomal dominant inheritance of Gerhardt's syndrome in three generations of a family. G Morelli, C Mesolella, M L Cavaliere, M Stabile, and V Ventruto J Med Genet 1980; 17: 325. doi:10.1136/jmg.17.4.325-a [PDF] [Request Permissions]
	Tuberous Sclerosis. R A Pagon J Med Genet 1980; 17: 325-326. doi:10.1136/jmg.17.4.325-b [PDF] [Request Permissions]
	Congenital hypothyroidism and Klinefelter's syndrome. F Harris J Med Genet 1980; 17: 326-327. doi:10.1136/jmg.17.4.326-a [PDF] [Request Permissions]