J Med Genet -- Table of Contents (18 [6])

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December 1981 (Volume 18, Number 6). [Index by author]

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Articles

Symmetrical infantile thalamic degeneration in two sibs
Dianne N Abuelo, Gail Barsel-Bowers, Barbara G Tutschka, Mary Ambler, and Don B Singer
J Med Genet 1981; 18: 448-450. doi:10.1136/jmg.18.6.448 [Abstract] [PDF] [Request Permissions]

Research Article

The development of clinical genetics.
A W Johnston
J Med Genet 1981; 18: 405-409. doi:10.1136/jmg.18.6.405 [PDF] [Request Permissions]

Genes for super-intelligence?
J A Sofaer and A E Emery
J Med Genet 1981; 18: 410-413. doi:10.1136/jmg.18.6.410 [Abstract] [PDF] [Request Permissions]

Retardation of ovarian growth in male-sterile mice carrying an autosomal translocation.
U Mittwoch, S Mahadevaiah, and M B Olive
J Med Genet 1981; 18: 414-417. doi:10.1136/jmg.18.6.414 [Abstract] [PDF] [Request Permissions]

Trehalase activity in genetically diabetic mice (serum, kidney, and liver).
F C Baumann, F Boizard-Callais, and J Labat-Robert
J Med Genet 1981; 18: 418-423. doi:10.1136/jmg.18.6.418 [Abstract] [PDF] [Request Permissions]

Are congenital vertebral anomalies and spina bifida cystica aetiologically related?
R G Lendon, R Wynne-Davies, and M Lendon
J Med Genet 1981; 18: 424-427. doi:10.1136/jmg.18.6.424 [Abstract] [PDF] [Request Permissions]

Hereditary multiple exostoses: report of a kindred.
S L Gordon, J R Buchanan, and R L Ladda
J Med Genet 1981; 18: 428-430. doi:10.1136/jmg.18.6.428 [Abstract] [PDF] [Request Permissions]

Autosomal dominant hypoparathyroidism: a proband with concurrent nephrogenic diabetes insipidus.
A G Hunter, H Heick, W J Poznanski, and P N McLaine
J Med Genet 1981; 18: 431-435. doi:10.1136/jmg.18.6.431 [Abstract] [PDF] [Request Permissions]

Genetic aspects of autosomal dominant late onset cerebellar ataxia.
A E Harding
J Med Genet 1981; 18: 436-441. doi:10.1136/jmg.18.6.436 [Abstract] [PDF] [Request Permissions]

Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus.
M Zatz, A M Vianna-Morgante, P Campos, and A J Diament
J Med Genet 1981; 18: 442-447. doi:10.1136/jmg.18.6.442 [Abstract] [PDF] [Request Permissions]

Multiple pterygium syndrome.
V B Penchaszadeh and B Salszberg
J Med Genet 1981; 18: 451-455. doi:10.1136/jmg.18.6.451 [Abstract] [PDF] [Request Permissions]

Distal symphalangism associated with camptodactyly.
S Ohdo, Y Yamauchi, and K Hayakawa
J Med Genet 1981; 18: 456-458. doi:10.1136/jmg.18.6.456 [Abstract] [PDF] [Request Permissions]

A dental approach to carrier screening in X linked hypohidrotic ectodermal dysplasia.
J A Spfaer
J Med Genet 1981; 18: 459-460. doi:10.1136/jmg.18.6.459 [Abstract] [PDF] [Request Permissions]

HLA and renal transplantation: yet another approach.
A M MacLeod, R J Mason, and G R Catto
J Med Genet 1981; 18: 461-463. doi:10.1136/jmg.18.6.461 [Abstract] [PDF] [Request Permissions]

Cherchez les femmes (or the personal touch in the laboratory).
M J Seller
J Med Genet 1981; 18: 463-464. doi:10.1136/jmg.18.6.463 [PDF] [Request Permissions]

Partial proximal trisomy of the long arm of chromosome 5 (q13 leads to q22) resulting from maternal insertion der ins (10;5).
S Gilgenkrantz, P Dulucq, J L Bresson, A Gouget, C Pernot, and M J Gregoire
J Med Genet 1981; 18: 465-469. doi:10.1136/jmg.18.6.465 [Abstract] [PDF] [Request Permissions]

Partial trisomy 12q: report of a case and review.
S H Roberts, T Mattina, K M Laurence, G Sorge, and L Pavone
J Med Genet 1981; 18: 470-473. doi:10.1136/jmg.18.6.470 [Abstract] [PDF] [Request Permissions]

Unilateral radial aplasia and trisomy 22 mosaicism.
F Dulitzky, F Shabtal, J Zlotogora, I Halbrecht, and E Elian
J Med Genet 1981; 18: 473-476. doi:10.1136/jmg.18.6.473 [Abstract] [PDF] [Request Permissions]

Prenatal diagnosis of thalassaemia major resulting from Lepore/ beta-thalassaemia genotype.
M Furbetta, A Angius, A M Falchi, T Tuveri, Tannoia, A P Pertosa, and A Cao
J Med Genet 1981; 18: 476-478. doi:10.1136/jmg.18.6.476 [Abstract] [PDF] [Request Permissions]

A case of the orocraniodigital (Juberg-Hayward) syndrome.
N C Nevin, P Henry, and P T Thomas
J Med Genet 1981; 18: 478-480. doi:10.1136/jmg.18.6.478 [Abstract] [PDF] [Request Permissions]

A new case of Prader-Willi syndrome with chromosomal aberration.
S Moric-Petrovic, Z Laca, A Krstic, and M Zivkov
J Med Genet 1981; 18: 481. doi:10.1136/jmg.18.6.481 [PDF] [Request Permissions]

A female with XO/XY mosaicism and partial trisomy 9p.
M Klasen, I Hansmann, M Schmid, and J Schmidtke
J Med Genet 1981; 18: 482. doi:10.1136/jmg.18.6.482 [PDF] [Request Permissions]

Partial trisomy for long arm of chromosome 16.
K E Buckton and D G Barr
J Med Genet 1981; 18: 483. doi:10.1136/jmg.18.6.483 [PDF] [Request Permissions]

Season and interval for recurrence of neural tube defects.
B Field and C Kerr
J Med Genet 1981; 18: 484. doi:10.1136/jmg.18.6.484 [PDF] [Request Permissions]

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	Symmetrical infantile thalamic degeneration in two sibs Dianne N Abuelo, Gail Barsel-Bowers, Barbara G Tutschka, Mary Ambler, and Don B Singer J Med Genet 1981; 18: 448-450. doi:10.1136/jmg.18.6.448 [Abstract] [PDF] [Request Permissions]

	The development of clinical genetics. A W Johnston J Med Genet 1981; 18: 405-409. doi:10.1136/jmg.18.6.405 [PDF] [Request Permissions]

	Genes for super-intelligence? J A Sofaer and A E Emery J Med Genet 1981; 18: 410-413. doi:10.1136/jmg.18.6.410 [Abstract] [PDF] [Request Permissions]

	Retardation of ovarian growth in male-sterile mice carrying an autosomal translocation. U Mittwoch, S Mahadevaiah, and M B Olive J Med Genet 1981; 18: 414-417. doi:10.1136/jmg.18.6.414 [Abstract] [PDF] [Request Permissions]

	Trehalase activity in genetically diabetic mice (serum, kidney, and liver). F C Baumann, F Boizard-Callais, and J Labat-Robert J Med Genet 1981; 18: 418-423. doi:10.1136/jmg.18.6.418 [Abstract] [PDF] [Request Permissions]

	Are congenital vertebral anomalies and spina bifida cystica aetiologically related? R G Lendon, R Wynne-Davies, and M Lendon J Med Genet 1981; 18: 424-427. doi:10.1136/jmg.18.6.424 [Abstract] [PDF] [Request Permissions]

	Hereditary multiple exostoses: report of a kindred. S L Gordon, J R Buchanan, and R L Ladda J Med Genet 1981; 18: 428-430. doi:10.1136/jmg.18.6.428 [Abstract] [PDF] [Request Permissions]

	Autosomal dominant hypoparathyroidism: a proband with concurrent nephrogenic diabetes insipidus. A G Hunter, H Heick, W J Poznanski, and P N McLaine J Med Genet 1981; 18: 431-435. doi:10.1136/jmg.18.6.431 [Abstract] [PDF] [Request Permissions]

	Genetic aspects of autosomal dominant late onset cerebellar ataxia. A E Harding J Med Genet 1981; 18: 436-441. doi:10.1136/jmg.18.6.436 [Abstract] [PDF] [Request Permissions]

	Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus. M Zatz, A M Vianna-Morgante, P Campos, and A J Diament J Med Genet 1981; 18: 442-447. doi:10.1136/jmg.18.6.442 [Abstract] [PDF] [Request Permissions]

	Multiple pterygium syndrome. V B Penchaszadeh and B Salszberg J Med Genet 1981; 18: 451-455. doi:10.1136/jmg.18.6.451 [Abstract] [PDF] [Request Permissions]

	Distal symphalangism associated with camptodactyly. S Ohdo, Y Yamauchi, and K Hayakawa J Med Genet 1981; 18: 456-458. doi:10.1136/jmg.18.6.456 [Abstract] [PDF] [Request Permissions]

	A dental approach to carrier screening in X linked hypohidrotic ectodermal dysplasia. J A Spfaer J Med Genet 1981; 18: 459-460. doi:10.1136/jmg.18.6.459 [Abstract] [PDF] [Request Permissions]

	HLA and renal transplantation: yet another approach. A M MacLeod, R J Mason, and G R Catto J Med Genet 1981; 18: 461-463. doi:10.1136/jmg.18.6.461 [Abstract] [PDF] [Request Permissions]

	Cherchez les femmes (or the personal touch in the laboratory). M J Seller J Med Genet 1981; 18: 463-464. doi:10.1136/jmg.18.6.463 [PDF] [Request Permissions]

	Partial proximal trisomy of the long arm of chromosome 5 (q13 leads to q22) resulting from maternal insertion der ins (10;5). S Gilgenkrantz, P Dulucq, J L Bresson, A Gouget, C Pernot, and M J Gregoire J Med Genet 1981; 18: 465-469. doi:10.1136/jmg.18.6.465 [Abstract] [PDF] [Request Permissions]

	Partial trisomy 12q: report of a case and review. S H Roberts, T Mattina, K M Laurence, G Sorge, and L Pavone J Med Genet 1981; 18: 470-473. doi:10.1136/jmg.18.6.470 [Abstract] [PDF] [Request Permissions]

	Unilateral radial aplasia and trisomy 22 mosaicism. F Dulitzky, F Shabtal, J Zlotogora, I Halbrecht, and E Elian J Med Genet 1981; 18: 473-476. doi:10.1136/jmg.18.6.473 [Abstract] [PDF] [Request Permissions]

	Prenatal diagnosis of thalassaemia major resulting from Lepore/ beta-thalassaemia genotype. M Furbetta, A Angius, A M Falchi, T Tuveri, Tannoia, A P Pertosa, and A Cao J Med Genet 1981; 18: 476-478. doi:10.1136/jmg.18.6.476 [Abstract] [PDF] [Request Permissions]

	A case of the orocraniodigital (Juberg-Hayward) syndrome. N C Nevin, P Henry, and P T Thomas J Med Genet 1981; 18: 478-480. doi:10.1136/jmg.18.6.478 [Abstract] [PDF] [Request Permissions]

	A new case of Prader-Willi syndrome with chromosomal aberration. S Moric-Petrovic, Z Laca, A Krstic, and M Zivkov J Med Genet 1981; 18: 481. doi:10.1136/jmg.18.6.481 [PDF] [Request Permissions]

	A female with XO/XY mosaicism and partial trisomy 9p. M Klasen, I Hansmann, M Schmid, and J Schmidtke J Med Genet 1981; 18: 482. doi:10.1136/jmg.18.6.482 [PDF] [Request Permissions]

	Partial trisomy for long arm of chromosome 16. K E Buckton and D G Barr J Med Genet 1981; 18: 483. doi:10.1136/jmg.18.6.483 [PDF] [Request Permissions]

	Season and interval for recurrence of neural tube defects. B Field and C Kerr J Med Genet 1981; 18: 484. doi:10.1136/jmg.18.6.484 [PDF] [Request Permissions]