Craniofrontonasal dysplasia.
I D Young
J Med Genet 1987; 24: 193-196. doi:10.1136/jmg.24.4.193
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Localisation of Y chromosome sequences in normal and 'XX' males.
V J Buckle, Y Boyd, N Fraser, P N Goodfellow, P J Goodfellow, J Wolfe, and I W Craig
J Med Genet 1987; 24: 197-203. doi:10.1136/jmg.24.4.197
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A previously undescribed syndrome of thoracic dysplasia and communicating hydrocephalus in two sibs, one diagnosed prenatally by ultrasound.
R M Winter, S Campbell, J S Wigglesworth, and E J Nevrkla
J Med Genet 1987; 24: 204-206. doi:10.1136/jmg.24.4.204
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Prenatal diagnosis of X linked hydrocephalus without aqueductal stenosis.
V Váradi, K Csécsei, G T Szeifert, Z Tóth, and Z Papp
J Med Genet 1987; 24: 207-209. doi:10.1136/jmg.24.4.207
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Endocardial fibroelastosis: possible X linked inheritance.
S Hodgson, A Child, and M Dyson
J Med Genet 1987; 24: 210-214. doi:10.1136/jmg.24.4.210
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Inherited haemoglobin variants in a South African population.
A R Bird, P Ellis, K Wood, C Mathew, and C Karabus
J Med Genet 1987; 24: 215-219. doi:10.1136/jmg.24.4.215
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Ectrodactyly in sisters and half sisters.
M H Mufti and S K Wood
J Med Genet 1987; 24: 220-224. doi:10.1136/jmg.24.4.220
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Features of di George syndrome in a child with 45,XX,-3,-22,+der(3),t(3;22)(p25;q11).
M J Faed, J Robertson, J S Beck, J I Cater, B Bose, and M M Madlom
J Med Genet 1987; 24: 225-227. doi:10.1136/jmg.24.4.225
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A child with partial monosomy 6q secondary to a maternal direct insertional event.
S V Matkins, J E Meyer, and A C Berry
J Med Genet 1987; 24: 227-229. doi:10.1136/jmg.24.4.227
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Interstitial deletion 1p in a 30 year old woman.
M B Petersen and M Warburg
J Med Genet 1987; 24: 229-231. doi:10.1136/jmg.24.4.229
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A girl with the Weaver syndrome.
E M Thompson, S Hill, J V Leonard, and M E Pembrey
J Med Genet 1987; 24: 232-234. doi:10.1136/jmg.24.4.232
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