J Med Genet -- Table of Contents (27 [6])

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June 1990 (Volume 27, Number 6). [Index by author]

		Book Reviews Dysmorphology Report Research Article

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Book Reviews

Garrod's Inborn Factors in Disease
J V Leonard
J Med Genet 1990; 27: 407. doi:10.1136/jmg.27.6.407-a [PDF] [Request Permissions]

Handbook of Normal Physical Measurements
Dian Donnai
J Med Genet 1990; 27: 407. doi:10.1136/jmg.27.6.407-b [PDF] [Request Permissions]

Molecular Probes—Technology and Medical Applications
John F Harvey
J Med Genet 1990; 27: 407-408. doi:10.1136/jmg.27.6.407-c [PDF] [Request Permissions]

Dysmorphology Report

Unknown syndrome: radial ray defects, omphalocele, diaphragmatic hernia, and hepatic cyst
R Gershoni-Baruch, I Machoul, Y Weiss, and S Blazer
J Med Genet 1990; 27: 403-404. doi:10.1136/jmg.27.6.403 [Abstract] [PDF] [Request Permissions]

Research Article

Dystrophin expression and genotypic analysis of two cases of benign X linked myopathy (McLeod's syndrome).
N D Carter, J E Morgan, A P Monaco, M S Schwartz, and S Jeffery
J Med Genet 1990; 27: 345-347. doi:10.1136/jmg.27.6.345 [Abstract] [PDF] [Request Permissions]

Consanguinity and its effect on fetal growth and development: a south Indian study.
M L Kulkarni and M Kurian
J Med Genet 1990; 27: 348-352. doi:10.1136/jmg.27.6.348 [Abstract] [PDF] [Request Permissions]

Limb reduction defects in Emilia Romagna, Italy: epidemiological and genetic study in 173,109 consecutive births.
E Calzolari, D Manservigi, G P Garani, G Cocchi, C Magnani, and M Milan
J Med Genet 1990; 27: 353-357. doi:10.1136/jmg.27.6.353 [Abstract] [PDF] [Request Permissions]

Facial measurements in the newborn (towards syndrome delineation)
O O Omotade
J Med Genet 1990; 27: 358-362. doi:10.1136/jmg.27.6.358 [Abstract] [PDF] [Request Permissions]

Cosegregation of hypertrophic cardiomyopathy and a fragile site on chromosome 16 in a large Italian family.
M Ferraro, G Scarton, and M Ambrosini
J Med Genet 1990; 27: 363-366. doi:10.1136/jmg.27.6.363 [Abstract] [PDF] [Request Permissions]

Segregation analysis of dominant osteogenesis imperfecta in Italy.
M Mottes, L Cugola, N Cappello, and P F Pignatti
J Med Genet 1990; 27: 367-370. doi:10.1136/jmg.27.6.367 [Abstract] [PDF] [Request Permissions]

The Baller-Gerold syndrome: phenotypic and cytogenetic overlap with Roberts syndrome.
S M Huson, C S Rodgers, C M Hall, and R M Winter
J Med Genet 1990; 27: 371-375. doi:10.1136/jmg.27.6.371 [Abstract] [PDF] [Request Permissions]

Sex linked deafness: Wilde revisited.
W Reardon
J Med Genet 1990; 27: 376-379. doi:10.1136/jmg.27.6.376 [Abstract] [PDF] [Request Permissions]

Genetic services in Hong Kong.
A S Chau, S T Lam, and A Ghosh
J Med Genet 1990; 27: 380-383. doi:10.1136/jmg.27.6.380 [PDF] [Request Permissions]

Maxillonasal dysplasia (Binder's syndrome)
O W Quarrell, M Koch, and H E Hughes
J Med Genet 1990; 27: 384-387. doi:10.1136/jmg.27.6.384 [PDF] [Request Permissions]

A general diagram of the human genome.
R Cruz-Coke
J Med Genet 1990; 27: 388-389. doi:10.1136/jmg.27.6.388 [Abstract] [PDF] [Request Permissions]

CHILD + ILVEN = PEN or PENCIL.
C Moss and J Burn
J Med Genet 1990; 27: 390-391. doi:10.1136/jmg.27.6.390 [PDF] [Request Permissions]

Winglets of the eye: dominant transmission of early adult pterygium of the conjunctiva.
F Hecht and M G Shoptaugh
J Med Genet 1990; 27: 392-394. doi:10.1136/jmg.27.6.392 [Abstract] [PDF] [Request Permissions]

A further family with congenital renal proximal tubular dysgenesis.
P MacMahon, R A Blackie, M J House, R A Risdon, and M D Crawfurd
J Med Genet 1990; 27: 395-398. doi:10.1136/jmg.27.6.395 [Abstract] [PDF] [Request Permissions]

Proteus syndrome: report of a case with severe brain impairment and fatal course.
R Rizzo, L Pavone, G Sorge, E Parano, and M Baraitser
J Med Genet 1990; 27: 399-402. doi:10.1136/jmg.27.6.399 [Abstract] [PDF] [Request Permissions]

Cornelia de Lange syndrome with ring chromosome 3.
P Lakshminarayana and P Nallasivam
J Med Genet 1990; 27: 405-406. doi:10.1136/jmg.27.6.405 [PDF] [Request Permissions]

Prenatal exclusion testing for Huntington's disease.
S Dalby
J Med Genet 1990; 27: 407. doi:10.1136/jmg.27.6.407 [PDF] [Request Permissions]

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	Garrod's Inborn Factors in Disease J V Leonard J Med Genet 1990; 27: 407. doi:10.1136/jmg.27.6.407-a [PDF] [Request Permissions]

	Handbook of Normal Physical Measurements Dian Donnai J Med Genet 1990; 27: 407. doi:10.1136/jmg.27.6.407-b [PDF] [Request Permissions]

	Molecular Probes—Technology and Medical Applications John F Harvey J Med Genet 1990; 27: 407-408. doi:10.1136/jmg.27.6.407-c [PDF] [Request Permissions]

	Unknown syndrome: radial ray defects, omphalocele, diaphragmatic hernia, and hepatic cyst R Gershoni-Baruch, I Machoul, Y Weiss, and S Blazer J Med Genet 1990; 27: 403-404. doi:10.1136/jmg.27.6.403 [Abstract] [PDF] [Request Permissions]

	Dystrophin expression and genotypic analysis of two cases of benign X linked myopathy (McLeod's syndrome). N D Carter, J E Morgan, A P Monaco, M S Schwartz, and S Jeffery J Med Genet 1990; 27: 345-347. doi:10.1136/jmg.27.6.345 [Abstract] [PDF] [Request Permissions]

	Consanguinity and its effect on fetal growth and development: a south Indian study. M L Kulkarni and M Kurian J Med Genet 1990; 27: 348-352. doi:10.1136/jmg.27.6.348 [Abstract] [PDF] [Request Permissions]

	Limb reduction defects in Emilia Romagna, Italy: epidemiological and genetic study in 173,109 consecutive births. E Calzolari, D Manservigi, G P Garani, G Cocchi, C Magnani, and M Milan J Med Genet 1990; 27: 353-357. doi:10.1136/jmg.27.6.353 [Abstract] [PDF] [Request Permissions]

	Facial measurements in the newborn (towards syndrome delineation) O O Omotade J Med Genet 1990; 27: 358-362. doi:10.1136/jmg.27.6.358 [Abstract] [PDF] [Request Permissions]

	Cosegregation of hypertrophic cardiomyopathy and a fragile site on chromosome 16 in a large Italian family. M Ferraro, G Scarton, and M Ambrosini J Med Genet 1990; 27: 363-366. doi:10.1136/jmg.27.6.363 [Abstract] [PDF] [Request Permissions]

	Segregation analysis of dominant osteogenesis imperfecta in Italy. M Mottes, L Cugola, N Cappello, and P F Pignatti J Med Genet 1990; 27: 367-370. doi:10.1136/jmg.27.6.367 [Abstract] [PDF] [Request Permissions]

	The Baller-Gerold syndrome: phenotypic and cytogenetic overlap with Roberts syndrome. S M Huson, C S Rodgers, C M Hall, and R M Winter J Med Genet 1990; 27: 371-375. doi:10.1136/jmg.27.6.371 [Abstract] [PDF] [Request Permissions]

	Sex linked deafness: Wilde revisited. W Reardon J Med Genet 1990; 27: 376-379. doi:10.1136/jmg.27.6.376 [Abstract] [PDF] [Request Permissions]

	Genetic services in Hong Kong. A S Chau, S T Lam, and A Ghosh J Med Genet 1990; 27: 380-383. doi:10.1136/jmg.27.6.380 [PDF] [Request Permissions]

	Maxillonasal dysplasia (Binder's syndrome) O W Quarrell, M Koch, and H E Hughes J Med Genet 1990; 27: 384-387. doi:10.1136/jmg.27.6.384 [PDF] [Request Permissions]

	A general diagram of the human genome. R Cruz-Coke J Med Genet 1990; 27: 388-389. doi:10.1136/jmg.27.6.388 [Abstract] [PDF] [Request Permissions]

	CHILD + ILVEN = PEN or PENCIL. C Moss and J Burn J Med Genet 1990; 27: 390-391. doi:10.1136/jmg.27.6.390 [PDF] [Request Permissions]

	Winglets of the eye: dominant transmission of early adult pterygium of the conjunctiva. F Hecht and M G Shoptaugh J Med Genet 1990; 27: 392-394. doi:10.1136/jmg.27.6.392 [Abstract] [PDF] [Request Permissions]

	A further family with congenital renal proximal tubular dysgenesis. P MacMahon, R A Blackie, M J House, R A Risdon, and M D Crawfurd J Med Genet 1990; 27: 395-398. doi:10.1136/jmg.27.6.395 [Abstract] [PDF] [Request Permissions]

	Proteus syndrome: report of a case with severe brain impairment and fatal course. R Rizzo, L Pavone, G Sorge, E Parano, and M Baraitser J Med Genet 1990; 27: 399-402. doi:10.1136/jmg.27.6.399 [Abstract] [PDF] [Request Permissions]

	Cornelia de Lange syndrome with ring chromosome 3. P Lakshminarayana and P Nallasivam J Med Genet 1990; 27: 405-406. doi:10.1136/jmg.27.6.405 [PDF] [Request Permissions]

	Prenatal exclusion testing for Huntington's disease. S Dalby J Med Genet 1990; 27: 407. doi:10.1136/jmg.27.6.407 [PDF] [Request Permissions]