Ataxia-Telangiectasia. A Cellular and Molecular Link Between Cancer, Neuropathology, and Immune Deficiency
S Bundey
J Med Genet 1984; 21: 475. doi:10.1136/jmg.21.6.475
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Heritable Disorders of Connective Tissue
F M Pope
J Med Genet 1984; 21: 475-476. doi:10.1136/jmg.21.6.475-a
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Issues and Reviews in Teratology
F Beck
J Med Genet 1984; 21: 476. doi:10.1136/jmg.21.6.476
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Blood Relations. Blood Groups and Anthropology
D F Roberts
J Med Genet 1984; 21: 476-477. doi:10.1136/jmg.21.6.476-a
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Research Ethics
I D Young
J Med Genet 1984; 21: 477. doi:10.1136/jmg.21.6.477
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Annual Review of Genetics
Andrew P Read
J Med Genet 1984; 21: 478. doi:10.1136/jmg.21.6.478
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Utilization of Mammalian Specific Locus Studies in Hazard Evaluation and Estimation of Genetic Risk
B M Cattanach
J Med Genet 1984; 21: 478-479. doi:10.1136/jmg.21.6.478-a
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Paracentric inversions in man.
K Madan, M Seabright, R H Lindenbaum, and M Bobrow
J Med Genet 1984; 21: 407-412. doi:10.1136/jmg.21.6.407
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Recurrence risk after neural tube defects in a genetic counselling clinic.
A Czeizel and J Métneki
J Med Genet 1984; 21: 413-416. doi:10.1136/jmg.21.6.413
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A study of retinitis pigmentosa in the City of Birmingham. I Prevalence.
S Bundey and S J Crews
J Med Genet 1984; 21: 417-420. doi:10.1136/jmg.21.6.417
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A study of retinitis pigmentosa in the City of Birmingham. II Clinical and genetic heterogeneity.
S Bundey and S J Crews
J Med Genet 1984; 21: 421-428. doi:10.1136/jmg.21.6.421
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A linkage study between HLA and cutaneous malignant melanoma or precursor lesions or both.
F Demenais, J P Cesarini, M Daveau, B Cavelier, J Gony, N Feingold, and J Hors
J Med Genet 1984; 21: 429-435. doi:10.1136/jmg.21.6.429
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An epidemiological and genetic study of facial clefting in France. II Segregation analysis.
F Demenais, C Bonaïti-Pellié, M L Briard, and J Feingold
J Med Genet 1984; 21: 436-440. doi:10.1136/jmg.21.6.436
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Glycoproteins in cystic fibrosis: a lectin binding study.
S Karlsson, B Griffiths, D M Swallow, D A Hopkinson, and P G Wallis
J Med Genet 1984; 21: 441-446. doi:10.1136/jmg.21.6.441
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Chronic proximal spinal muscular atrophy of childhood and adolescence: sex influence.
I Hausmanowa-Petrusewicz, J Zaremba, J Borkowska, and W Szirkowiec
J Med Genet 1984; 21: 447-450. doi:10.1136/jmg.21.6.447
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Familial paracentric inversion of chromosome 15 (q15q24).
G Del Porto, E D'Alessandro, C De Matteis, R D'Innocenzo, M Baldi, A Pachi, and F Cappa
J Med Genet 1984; 21: 451-453. doi:10.1136/jmg.21.6.451
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A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter.
R Voss, E Gross-Kieselstein, H Hurvitz, J Dagan, E Kerem, and J Zlotogora
J Med Genet 1984; 21: 454-459. doi:10.1136/jmg.21.6.454
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Stub thumbs in Israel revisited.
R M Goodman, A Feinstein, and M Hertz
J Med Genet 1984; 21: 460-462. doi:10.1136/jmg.21.6.460
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Paternal Robertsonian translocation t(13q;14q) and maternal reciprocal translocation t(7p;13q) in a couple with repeated fetal loss.
P R Scarbrough, A J Carroll, J B Younger, and S C Finley
J Med Genet 1984; 21: 463-464. doi:10.1136/jmg.21.6.463
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Interstitial deletion of the short arm of chromosome 5 in a mother and three children.
J L Walker, C E Blank, and B A Smith
J Med Genet 1984; 21: 465-467. doi:10.1136/jmg.21.6.465
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A live infant with trisomy 14 mosaicism and nuclear abnormalities of the neutrophils.
B Dallapiccola, G Ferranti, A Giannotti, G Novelli, L Pasquini, and B Porfirio
J Med Genet 1984; 21: 467-470. doi:10.1136/jmg.21.6.467
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A rare heterochromatic variant of chromosome 4.
Z Docherty and S M Bowser-Riley
J Med Genet 1984; 21: 470-472. doi:10.1136/jmg.21.6.470
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Prevention of midline defects.
J U Walther and J A Raeburn
J Med Genet 1984; 21: 473-474. doi:10.1136/jmg.21.6.473-a
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Translocations, social class, and Adam and Eve.
R J Gardner
J Med Genet 1984; 21: 474. doi:10.1136/jmg.21.6.474
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Tracheo-oesophageal dysraphism.
F C Fraser
J Med Genet 1984; 21: 474. doi:10.1136/jmg.21.6.474-a
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