Colchester revisited: a genetic study of mental defect.
N E Morton, D C Rao, H Lang-Brown, C J Maclean, R D Bart, and R Lew
J Med Genet 1977; 14: 1-9. doi:10.1136/jmg.14.1.1
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Height and seriousness of crime in XYY men.
E B Hook and K M Healy
J Med Genet 1977; 14: 10-12. doi:10.1136/jmg.14.1.10
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Muscle nuclear changes in fetuses at risk for Duchenne muscular dystrophy.
D Vassilopoulos and A E Emery
J Med Genet 1977; 14: 13-15. doi:10.1136/jmg.14.1.13
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Immunoglobulin levels in dystrophia myotonica.
D F Roberts and W G Bradley
J Med Genet 1977; 14: 16-19. doi:10.1136/jmg.14.1.16
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Heterozygote advantage for the phenylketonuria allele.
L F Saugstad
J Med Genet 1977; 14: 20-24. doi:10.1136/jmg.14.1.20
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A simple non-graphic method for pedigree description and analysis.
T Schaap and M M Cohen
J Med Genet 1977; 14: 25-29. doi:10.1136/jmg.14.1.25
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Unusual occurrence of dextrocardia with situs inversus in succeeding generations of a family.
P Chib, D N Grover, and B N Shahi
J Med Genet 1977; 14: 30-32. doi:10.1136/jmg.14.1.30
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Two cases of Ellis-van Creveld syndrome in a small island population.
R D Hill
J Med Genet 1977; 14: 33-36. doi:10.1136/jmg.14.1.33
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Prenatal diagnosis: techniques used to help in ruling out maternal cell contamination.
D C Peakman, M F Moreton, and A Robinson
J Med Genet 1977; 14: 37-39. doi:10.1136/jmg.14.1.37
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A fluorescence polymorphism associated with Down's syndrome?
J A Robinson and M Newton
J Med Genet 1977; 14: 40-45. doi:10.1136/jmg.14.1.40
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Familial X-linked mental retardation with an X chromosome abnormality.
J Harvey, C Judge, and S Wiener
J Med Genet 1977; 14: 46-50. doi:10.1136/jmg.14.1.46
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Myotonic dystrophy, syringomyelia, and 2/13 translocation in the same family.
R B Levisky, A M Vianna-Morgante, O Frota-Pessoa, M Scaff, A M Tsanaclis, and J A Levy
J Med Genet 1977; 14: 51-53. doi:10.1136/jmg.14.1.51
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Four new cases of ring 21 and 22 including familial transmission of ring 21.
C G Palmer, M E Hodes, T Reed, and J Kojetin
J Med Genet 1977; 14: 54-60. doi:10.1136/jmg.14.1.54
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Physical retardation is associated with ring chromosome mosaicism: 46, XX,r(10)/45, XX,10 minus.
S Lansky, W Daniel, and K Fleiszar
J Med Genet 1977; 14: 61-63. doi:10.1136/jmg.14.1.61
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46,XX/46,XX,r(15) mosaiciam: report of a case.
R A Pfeiffer, R Dhadial, and W Lenz
J Med Genet 1977; 14: 63-65. doi:10.1136/jmg.14.1.63
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Stable dicentric autosome, tdic (8:22)(p23:p13), in a mentally retarded girl.
S H Roberts, R T Howell, K M Laurence, and M E Heathcote
J Med Genet 1977; 14: 66-68. doi:10.1136/jmg.14.1.66
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Mental retardation with 45 chromosomes 45,XX,--5,--14,+der(5) t(5,14)(p15;q13) mat due to familial balanced reciprocal translocation.
K Fried, M Tieder, S Beer, M Rosenblatt, and H I Krespin
J Med Genet 1977; 14: 68-72. doi:10.1136/jmg.14.1.68
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Sex linked hydrocephalus.
R Cassie and A R Boon
J Med Genet 1977; 14: 72-73. doi:10.1136/jmg.14.1.72
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Crossed asymmetry in Russell-Silver syndrome.
Q H Qazi, E G Kassner, and C Ganapathy
J Med Genet 1977; 14: 74-75. doi:10.1136/jmg.14.1.74
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A new syndrome of cleft palate associated with coloboma, hypospadias, deafness, short stature, and radial synostosis.
M A Abruzzo and R P Erickson
J Med Genet 1977; 14: 76-80. doi:10.1136/jmg.14.1.76
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