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December 1974 (Volume 11, Number 4). [Index by author]

		Articles Miscellaneous Articles Case Reports Research Article Short Communications

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Articles

Linkage between the loci for benign (Becker-type) X-borne muscular dystrophy and deutan colour blindness
Rosalind Skinner, Charles Smith, and Alan E. H. Emery
J Med Genet 1974; 11: 317-320. doi:10.1136/jmg.11.4.317 [Abstract] [PDF] [Request Permissions]

New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups
Mayana Zatz, Sueli B. Itskan, Ruth Sanger, O. Frota-Pessoa, and P. H. Saldanha
J Med Genet 1974; 11: 321-327. doi:10.1136/jmg.11.4.321 [Abstract] [PDF] [Request Permissions]

Racial variation in diabetes mellitus in Japanese and Caucasians living in Hawaii
Madeleine J. Goodman, Chin S. Chung, and Fred Gilbert, Jr
J Med Genet 1974; 11: 328-334. doi:10.1136/jmg.11.4.328 [Abstract] [PDF] [Request Permissions]

Absence of the ${alpha}$ -thalassaemia syndromes in Egyptian Arabs
O. Selim, K. Kamel, F. Sabry, A. Ibrahim, and D. J. Weatherall
J Med Genet 1974; 11: 335-336. doi:10.1136/jmg.11.4.335 [Abstract] [PDF] [Request Permissions]

${delta}$ β-Thalassaemia in two Turkish families
Muzaffer Aksoy, SNakir Erdem, and Günçag Dinçol
J Med Genet 1974; 11: 337-340. doi:10.1136/jmg.11.4.337 [Abstract] [PDF] [Request Permissions]

Haemoglobin D Punjab (D Los Angeles)
F. Vella and H. Lehmann
J Med Genet 1974; 11: 341-348. doi:10.1136/jmg.11.4.341 [Abstract] [PDF] [Request Permissions]

Haptoglobins in chronic lymphatic leukaemia
S. S. Papiha, A. L. Jones, B. Thompson, and D. Carr
J Med Genet 1974; 11: 349-352. doi:10.1136/jmg.11.4.349 [Abstract] [PDF] [Request Permissions]

Familial mental retardation in a family with an inherited chromosome rearrangement
A. E. Chudley, F. Bauder, M. Ray, Phyllis J. McAlpine, S. D. J. Pena, and J. L. Hamerton
J Med Genet 1974; 11: 353-366. doi:10.1136/jmg.11.4.353 [Abstract] [PDF] [Request Permissions]

Prenatal evaluation in a case of familial Y chromosome long arm deletion (Yq—)
M. Neil Macintyre, Ronald C. Rustad, and Karen Boerger Turk
J Med Genet 1974; 11: 367-370. doi:10.1136/jmg.11.4.367 [Abstract] [PDF] [Request Permissions]

Chromocentres in polymorphs as interphase markers for chromosomes having increased constitutive heterochromatin
N. B. Atkin and Marion C. Baker
J Med Genet 1974; 11: 371-373. doi:10.1136/jmg.11.4.371 [Abstract] [PDF] [Request Permissions]

Risk tables for genetic counselling in some common congenital malformations
Catherine Bonaiti-Pellié and Charles Smith
J Med Genet 1974; 11: 374-377. doi:10.1136/jmg.11.4.374 [Abstract] [PDF] [Request Permissions]

SI Units
J Med Genet 1974; 11: 381. doi:10.1136/jmg.11.4.381 [PDF] [Request Permissions]

Miscellaneous

Correction
J Med Genet 1974; 11: 410. doi:10.1136/jmg.11.4.410 [PDF] [Request Permissions]

Case Reports

Xerodermic idiocy in identical twins
L. Raju and B. A. Adam
J Med Genet 1974; 11: 382-384. doi:10.1136/jmg.11.4.382 [Abstract] [PDF] [Request Permissions]

Progeria in twins
Judith Viégas, P. L. R. Souza, and F. M. Salzano
J Med Genet 1974; 11: 384-386. doi:10.1136/jmg.11.4.384 [Abstract] [PDF] [Request Permissions]

21 Monosomy in a retarded female infant
Katherine H. Halloran, W. Roy Breg, and Maurice J. Mahoney
J Med Genet 1974; 11: 386-389. doi:10.1136/jmg.11.4.386 [Abstract] [PDF] [Request Permissions]

Karyotype 45,XX,–21/46,XX,21q– in an infant with symptoms of G-deletion syndrome I
Margareta Mikkelsen and S. Vestermark
J Med Genet 1974; 11: 389-393. doi:10.1136/jmg.11.4.389 [Abstract] [PDF] [Request Permissions]

The trisomy 8 syndrome: two additional mosaic cases
B. F. Crandall, H. N. Bass, S. M. Marcy, M. Glovsky, and C. H. Fish
J Med Genet 1974; 11: 393-398. doi:10.1136/jmg.11.4.393 [Abstract] [PDF] [Request Permissions]

Prenatal detection of D trisomy
K. M. Laurence, P. J. Gregory, and F. Sharp
J Med Genet 1974; 11: 398-400. doi:10.1136/jmg.11.4.398 [Abstract] [PDF] [Request Permissions]

A case of partial trisomy 15
E. Janet Watson and R. R. Gordon
J Med Genet 1974; 11: 400-402. doi:10.1136/jmg.11.4.400 [Abstract] [PDF] [Request Permissions]

Turner's syndrome and 46,X,i(Yq) karyotype
Norma C. Magnelli, Angela M. Vianna-Morgante, O. Frota-Pessoa, and Manuel Gonzalo Taboada-Lopez
J Med Genet 1974; 11: 403-406. doi:10.1136/jmg.11.4.403 [Abstract] [PDF] [Request Permissions]

Research Article

Three generations and seven family members with a t(21q22q) chromosome.
L Zergollern
J Med Genet 1974; 11: 379-381. doi:10.1136/jmg.11.4.379 [PDF] [Request Permissions]

Chromosomal abnormality associated with congenital macroglossia and other abnormalities.
G F Smith, S Sachdeva, N Janakiraman, and S N Sinha
J Med Genet 1974; 11: 406-410. doi:10.1136/jmg.11.4.406 [PDF] [Request Permissions]

Short Communications

Trisomy 21 mosaicism in a woman with two children with trisomy 21 Down's syndrome
Sara Kaffe, Lillian Y. F. Hsu, and Kurt Hirschhorn
J Med Genet 1974; 11: 378-379. doi:10.1136/jmg.11.4.378 [Abstract] [PDF] [Request Permissions]

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	Linkage between the loci for benign (Becker-type) X-borne muscular dystrophy and deutan colour blindness Rosalind Skinner, Charles Smith, and Alan E. H. Emery J Med Genet 1974; 11: 317-320. doi:10.1136/jmg.11.4.317 [Abstract] [PDF] [Request Permissions]

	New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups Mayana Zatz, Sueli B. Itskan, Ruth Sanger, O. Frota-Pessoa, and P. H. Saldanha J Med Genet 1974; 11: 321-327. doi:10.1136/jmg.11.4.321 [Abstract] [PDF] [Request Permissions]

	Racial variation in diabetes mellitus in Japanese and Caucasians living in Hawaii Madeleine J. Goodman, Chin S. Chung, and Fred Gilbert, Jr J Med Genet 1974; 11: 328-334. doi:10.1136/jmg.11.4.328 [Abstract] [PDF] [Request Permissions]

	Absence of the ${alpha}$ -thalassaemia syndromes in Egyptian Arabs O. Selim, K. Kamel, F. Sabry, A. Ibrahim, and D. J. Weatherall J Med Genet 1974; 11: 335-336. doi:10.1136/jmg.11.4.335 [Abstract] [PDF] [Request Permissions]

	${delta}$ β-Thalassaemia in two Turkish families Muzaffer Aksoy, SNakir Erdem, and Günçag Dinçol J Med Genet 1974; 11: 337-340. doi:10.1136/jmg.11.4.337 [Abstract] [PDF] [Request Permissions]

	Haemoglobin D Punjab (D Los Angeles) F. Vella and H. Lehmann J Med Genet 1974; 11: 341-348. doi:10.1136/jmg.11.4.341 [Abstract] [PDF] [Request Permissions]

	Haptoglobins in chronic lymphatic leukaemia S. S. Papiha, A. L. Jones, B. Thompson, and D. Carr J Med Genet 1974; 11: 349-352. doi:10.1136/jmg.11.4.349 [Abstract] [PDF] [Request Permissions]

	Familial mental retardation in a family with an inherited chromosome rearrangement A. E. Chudley, F. Bauder, M. Ray, Phyllis J. McAlpine, S. D. J. Pena, and J. L. Hamerton J Med Genet 1974; 11: 353-366. doi:10.1136/jmg.11.4.353 [Abstract] [PDF] [Request Permissions]

	Prenatal evaluation in a case of familial Y chromosome long arm deletion (Yq—) M. Neil Macintyre, Ronald C. Rustad, and Karen Boerger Turk J Med Genet 1974; 11: 367-370. doi:10.1136/jmg.11.4.367 [Abstract] [PDF] [Request Permissions]

	Chromocentres in polymorphs as interphase markers for chromosomes having increased constitutive heterochromatin N. B. Atkin and Marion C. Baker J Med Genet 1974; 11: 371-373. doi:10.1136/jmg.11.4.371 [Abstract] [PDF] [Request Permissions]

	Risk tables for genetic counselling in some common congenital malformations Catherine Bonaiti-Pellié and Charles Smith J Med Genet 1974; 11: 374-377. doi:10.1136/jmg.11.4.374 [Abstract] [PDF] [Request Permissions]

	SI Units J Med Genet 1974; 11: 381. doi:10.1136/jmg.11.4.381 [PDF] [Request Permissions]

	Correction J Med Genet 1974; 11: 410. doi:10.1136/jmg.11.4.410 [PDF] [Request Permissions]

	Xerodermic idiocy in identical twins L. Raju and B. A. Adam J Med Genet 1974; 11: 382-384. doi:10.1136/jmg.11.4.382 [Abstract] [PDF] [Request Permissions]

	Progeria in twins Judith Viégas, P. L. R. Souza, and F. M. Salzano J Med Genet 1974; 11: 384-386. doi:10.1136/jmg.11.4.384 [Abstract] [PDF] [Request Permissions]

	21 Monosomy in a retarded female infant Katherine H. Halloran, W. Roy Breg, and Maurice J. Mahoney J Med Genet 1974; 11: 386-389. doi:10.1136/jmg.11.4.386 [Abstract] [PDF] [Request Permissions]

	Karyotype 45,XX,–21/46,XX,21q– in an infant with symptoms of G-deletion syndrome I Margareta Mikkelsen and S. Vestermark J Med Genet 1974; 11: 389-393. doi:10.1136/jmg.11.4.389 [Abstract] [PDF] [Request Permissions]

	The trisomy 8 syndrome: two additional mosaic cases B. F. Crandall, H. N. Bass, S. M. Marcy, M. Glovsky, and C. H. Fish J Med Genet 1974; 11: 393-398. doi:10.1136/jmg.11.4.393 [Abstract] [PDF] [Request Permissions]

	Prenatal detection of D trisomy K. M. Laurence, P. J. Gregory, and F. Sharp J Med Genet 1974; 11: 398-400. doi:10.1136/jmg.11.4.398 [Abstract] [PDF] [Request Permissions]

	A case of partial trisomy 15 E. Janet Watson and R. R. Gordon J Med Genet 1974; 11: 400-402. doi:10.1136/jmg.11.4.400 [Abstract] [PDF] [Request Permissions]

	Turner's syndrome and 46,X,i(Yq) karyotype Norma C. Magnelli, Angela M. Vianna-Morgante, O. Frota-Pessoa, and Manuel Gonzalo Taboada-Lopez J Med Genet 1974; 11: 403-406. doi:10.1136/jmg.11.4.403 [Abstract] [PDF] [Request Permissions]

	Three generations and seven family members with a t(21q22q) chromosome. L Zergollern J Med Genet 1974; 11: 379-381. doi:10.1136/jmg.11.4.379 [PDF] [Request Permissions]

	Chromosomal abnormality associated with congenital macroglossia and other abnormalities. G F Smith, S Sachdeva, N Janakiraman, and S N Sinha J Med Genet 1974; 11: 406-410. doi:10.1136/jmg.11.4.406 [PDF] [Request Permissions]

	Trisomy 21 mosaicism in a woman with two children with trisomy 21 Down's syndrome Sara Kaffe, Lillian Y. F. Hsu, and Kurt Hirschhorn J Med Genet 1974; 11: 378-379. doi:10.1136/jmg.11.4.378 [Abstract] [PDF] [Request Permissions]