Congenital limb anomalies: frequency and aetiological factors: Data from the Edinburgh Register of the Newborn (1964-68)
E. J. Rogala, R. Wynne-Davies, A. Littlejohn, and J. Gormley
J Med Genet 1974; 11: 221-233. doi:10.1136/jmg.11.3.221
[Abstract]
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Comments upon the classification of infantile polycystic diseases of the liver and kidney, based upon three-dimensional reconstruction of the liver
Caroline M. Adams, D. M. Danks, and P. E. Campbell
J Med Genet 1974; 11: 234-243. doi:10.1136/jmg.11.3.234
[Abstract]
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Pleiotropic effects of the gene for retinoblastoma
F. D. Kitchin and Robert M. Ellsworth
J Med Genet 1974; 11: 244-246. doi:10.1136/jmg.11.3.244
[Abstract]
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Prenatal diagnosis: a problem in verification
Gertrude Kohn, Asher Ornoy, and Maimon M. Cohen
J Med Genet 1974; 11: 247-248. doi:10.1136/jmg.11.3.247
[Abstract]
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Effects of cystic fibrosis sera on Proteus vulgaris motility
F. L. Cohen and W. L. Daniel
J Med Genet 1974; 11: 253-256. doi:10.1136/jmg.11.3.253
[Abstract]
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Mitochondrial inclusions in fibroblast culture from a patient with β-methylcrotonylglycinuria
J. McLean and G. Stewart
J Med Genet 1974; 11: 257-259. doi:10.1136/jmg.11.3.257
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Effects of mitochondrial inhibition by chloramphenicol on the mitotic cycle of human cell cultures
Ursula Mittwoch, D. J. Kirk, and D. Wilkie
J Med Genet 1974; 11: 260-266. doi:10.1136/jmg.11.3.260
[Abstract]
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Clinical variations of testicular intersexuality in a family
S. Gardó and Z. Papp
J Med Genet 1974; 11: 267-270. doi:10.1136/jmg.11.3.267
[Abstract]
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Familial thyroxine-binding globulin deficiency: search for linkage with Xg blood groups
D. B. Grant, H. G. Minchin Clarke, and D. Putman
J Med Genet 1974; 11: 271-274. doi:10.1136/jmg.11.3.271
[Abstract]
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Haemoglobin H disease and β-thalassaemia: Clinical haematological and electrophoretic studies in a family from South Lebanon
Munib J. Shahid, Farid P. Khouri, and Itaf F. Sahli
J Med Genet 1974; 11: 275-279. doi:10.1136/jmg.11.3.275
[Abstract]
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Familial translocation 15/22. A possible cause for abortions in female carriers
K. Fried, J. Bukovsky, M. Rosenblatt, and G. Mundel
J Med Genet 1974; 11: 280-282. doi:10.1136/jmg.11.3.280
[Abstract]
[PDF]
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Congenital limb anomalies: frequency and aetiological factors: Data from the Edinburgh Register of the Newborn (1964-68)
E. J. Rogala, R. Wynne-Davies, A. Littlejohn, and J. Gormley
J Med Genet 1974; 11: 221-233. doi:10.1136/jmg.11.3.221
[Abstract]
[PDF]
[Request Permissions]
Comments upon the classification of infantile polycystic diseases of the liver and kidney, based upon three-dimensional reconstruction of the liver
Caroline M. Adams, D. M. Danks, and P. E. Campbell
J Med Genet 1974; 11: 234-243. doi:10.1136/jmg.11.3.234
[Abstract]
[PDF]
[Request Permissions]
Pleiotropic effects of the gene for retinoblastoma
F. D. Kitchin and Robert M. Ellsworth
J Med Genet 1974; 11: 244-246. doi:10.1136/jmg.11.3.244
[Abstract]
[PDF]
[Request Permissions]
Prenatal diagnosis: a problem in verification
Gertrude Kohn, Asher Ornoy, and Maimon M. Cohen
J Med Genet 1974; 11: 247-248. doi:10.1136/jmg.11.3.247
[Abstract]
[PDF]
[Request Permissions]
Effects of cystic fibrosis sera on Proteus vulgaris motility
F. L. Cohen and W. L. Daniel
J Med Genet 1974; 11: 253-256. doi:10.1136/jmg.11.3.253
[Abstract]
[PDF]
[Request Permissions]
Mitochondrial inclusions in fibroblast culture from a patient with β-methylcrotonylglycinuria
J. McLean and G. Stewart
J Med Genet 1974; 11: 257-259. doi:10.1136/jmg.11.3.257
[Abstract]
[PDF]
[Request Permissions]
Effects of mitochondrial inhibition by chloramphenicol on the mitotic cycle of human cell cultures
Ursula Mittwoch, D. J. Kirk, and D. Wilkie
J Med Genet 1974; 11: 260-266. doi:10.1136/jmg.11.3.260
[Abstract]
[PDF]
[Request Permissions]
Clinical variations of testicular intersexuality in a family
S. Gardó and Z. Papp
J Med Genet 1974; 11: 267-270. doi:10.1136/jmg.11.3.267
[Abstract]
[PDF]
[Request Permissions]
Familial thyroxine-binding globulin deficiency: search for linkage with Xg blood groups
D. B. Grant, H. G. Minchin Clarke, and D. Putman
J Med Genet 1974; 11: 271-274. doi:10.1136/jmg.11.3.271
[Abstract]
[PDF]
[Request Permissions]
Haemoglobin H disease and β-thalassaemia: Clinical haematological and electrophoretic studies in a family from South Lebanon
Munib J. Shahid, Farid P. Khouri, and Itaf F. Sahli
J Med Genet 1974; 11: 275-279. doi:10.1136/jmg.11.3.275
[Abstract]
[PDF]
[Request Permissions]
Familial translocation 15/22. A possible cause for abortions in female carriers
K. Fried, J. Bukovsky, M. Rosenblatt, and G. Mundel
J Med Genet 1974; 11: 280-282. doi:10.1136/jmg.11.3.280
[Abstract]
[PDF]
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Another human chimaera
Diana A. Battey, G. W. G. Bird, A. McDermott, C. W. Mortimer, O. M. Mutchinick, and June Wingham
J Med Genet 1974; 11: 283-287. doi:10.1136/jmg.11.3.283
[Abstract]
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Inherited partial duplication of chromosome No. 15
Atsuko Fujimoto, Joseph W. Towner, Allan J. Ebbin, Emily J. Kahlstrom, and Miriam G. Wilson
J Med Genet 1974; 11: 287-291. doi:10.1136/jmg.11.3.287
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Multiple congenital defects associated with trisomy for the short arm of chromosome 4
Lynne Owen, Barbara Martin, C. E. Blank, and F. Harris
J Med Genet 1974; 11: 291-295. doi:10.1136/jmg.11.3.291
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Histidinaemia in a consanguineous marriage
I. Rostenberg, J. Guïzar, I. Alejandre, S. Benïtez, and S. Armendares
J Med Genet 1974; 11: 296-297. doi:10.1136/jmg.11.3.296
[Abstract]
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A 21/21 tandem translocation with satellites on both long and short arms
Barbara E. Schuh, Bruce R. Korf, and Martin J. Salwen
J Med Genet 1974; 11: 297-299. doi:10.1136/jmg.11.3.297
[Abstract]
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Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother
N. Hobolth, Petrea Jacobsen, and Margareta Mikkelsen
J Med Genet 1974; 11: 299-303. doi:10.1136/jmg.11.3.299
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An unusual chromosomal segregation in a family with a translocation between chromosomes 3 and 12
Shanta Sachdeva, George F. Smith, and Parvin Justice
J Med Genet 1974; 11: 303-305. doi:10.1136/jmg.11.3.303
[Abstract]
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Down's syndrome associated with two Robertsonian translocations, 45,XX,–15,–21,+t(15q21q) and 46,XX,–21,+t(21q21q)
Leonard Atkins and Christos S. Bartsocas
J Med Genet 1974; 11: 306-309. doi:10.1136/jmg.11.3.306
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48,XXX, +18 double trisomy
D. P. Madahar, Harvey Dosik, and Irving Wexler
J Med Genet 1974; 11: 309-311. doi:10.1136/jmg.11.3.309
[Abstract]
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The tricho-rhino-phalangeal syndrome
David D. Weaver, M. Michael Cohen, and David W. Smith
J Med Genet 1974; 11: 312-314. doi:10.1136/jmg.11.3.312
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