Differentiation in human amniotic fluid cell cultures: I: Collagen production.
R E Priest, J H Priest, J F Moinuddin, and A J Keyser
J Med Genet 1977; 14: 157-162. doi:10.1136/jmg.14.3.157
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Differentiation in human amniotic fluid cell cultures: II: Secretion of an epithelial basement membrane glycoprotein.
J M Megaw, J H Priest, R E Priest, and L D Johnson
J Med Genet 1977; 14: 163-167. doi:10.1136/jmg.14.3.163
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Mild sickle-cell anaemia in Iran associated with high levels of fetal haemoglobin.
M Haghshenass, F Ismail-Beigi, J B Clegg, and D J Weatherall
J Med Genet 1977; 14: 168-171. doi:10.1136/jmg.14.3.168
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Genetic study of Welsh gypsies.
E M Williams and P R Harper
J Med Genet 1977; 14: 172-176. doi:10.1136/jmg.14.3.172
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Genetic markers in Welsh gypsies.
P S Harper, E M Williams, and E Sunderland
J Med Genet 1977; 14: 177-182. doi:10.1136/jmg.14.3.177
[Abstract]
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Alpha1-antitrypsin deficiency with M-like phenotype.
F Kueppers, G Utz, and B Simon
J Med Genet 1977; 14: 183-186. doi:10.1136/jmg.14.3.183
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Dermatoglyphs of Klinefelter's syndrome.
H Shiono, J Kadowaki, H Tanda, and M Hikita
J Med Genet 1977; 14: 187-189. doi:10.1136/jmg.14.3.187
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Diabetes mellitus, diabetes insipidus, and optic atrophy. An autosomal recessive syndrome?
F C Fraser and T Gunn
J Med Genet 1977; 14: 190-193. doi:10.1136/jmg.14.3.190
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Three sisters with gonadoblastoma.
B Ionescu and C Maximilian
J Med Genet 1977; 14: 194-199. doi:10.1136/jmg.14.3.194
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Inheritance of Ehlers-Danlos type IV syndrome.
F M Pope, G R Martin, and V A McKusick
J Med Genet 1977; 14: 200-204. doi:10.1136/jmg.14.3.200
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Bilateral absence of the kidneys and ureters. Three cases reported in one family.
H M Pashayan, T Dowd, and A V Nigro
J Med Genet 1977; 14: 205-209. doi:10.1136/jmg.14.3.205
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Xg groups and sex chromosome abnormalities in people of northern European ancestry: an addendum.
R Sanger, P Tippett, J Gavin, P Teesdale, and G L Daniels
J Med Genet 1977; 14: 210-211. doi:10.1136/jmg.14.3.210
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Association of ABO blood groups and vitiligo.
L Kareemullah, V Taneja, S Begum, P K Sarma, and H A Baig
J Med Genet 1977; 14: 211-213. doi:10.1136/jmg.14.3.211
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46,XX/47XX, + 14 mosaicism in a liveborn infant.
A O Martin, M M Ford, N T Khalil, K B Turk, and M N Macintyre
J Med Genet 1977; 14: 214-218. doi:10.1136/jmg.14.3.214
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45,X/47,XYY mosaicism.
M T Mulcahy, J Jenkyn, and A Mackellar
J Med Genet 1977; 14: 218-221. doi:10.1136/jmg.14.3.218
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Reproduction in a woman with low percentage t(21q21q) mosaicism.
H F Mark, T Mendoza, D Abuelo, L J Beauregard, J B May, and P H LaMarche
J Med Genet 1977; 14: 221-223. doi:10.1136/jmg.14.3.221
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Trisomy 22 mosaicism.
F Mollica, G Sorge, and L Pavone
J Med Genet 1977; 14: 224-225. doi:10.1136/jmg.14.3.224
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Twins with nonconcordant sexual aneuploidy.
J M Garcia-Sagredo, C Merello-Godino, and C San Roman
J Med Genet 1977; 14: 226-228. doi:10.1136/jmg.14.3.226
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Ring chromosome 4.
A McDermott, M A Voyce, and D Romain
J Med Genet 1977; 14: 228-232. doi:10.1136/jmg.14.3.228
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Prenatal recognition of 4p- syndrome.
S Blunt, A C Berry, M J Seller, and C A Williams
J Med Genet 1977; 14: 232-233. doi:10.1136/jmg.14.3.232
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Heterogeneity among ectodermal dysplasias.
N Freire-Maia
J Med Genet 1977; 14: 234. doi:10.1136/jmg.14.3.234
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