J Med Genet -- Table of Contents (24 [8])

Subscribe here
Activate your subscription

Home > Volume 24, Number 8

Only Abstracts and PDFs available for this issue

Other Issues:
August 1987 (Volume 24, Number 8). [Index by author]

		Correspondence Conference Reports Research Article

Find articles in this issue containing these words: [Search ALL Issues]

Table of Contents (PDF) | Cover (PDF) | Administration (PDF)

To see an article, click its [Full Text] link. To review many abstracts, check the boxes to the left of the titles you want, and click the 'Get All Checked Abstracts' button. To see one abstract at a time, click its [Abstract] link.

Correspondence

Correspondence
Michael Baraitser and Michael A Patton
J Med Genet 1987; 24: 511. doi:10.1136/jmg.24.8.511 [PDF] [Request Permissions]

Conference Reports

The Second Manchester Birth Defects Conference, 1 to 3 October 1986
John Burn
J Med Genet 1987; 24: 505-507. doi:10.1136/jmg.24.8.505 [PDF] [Request Permissions]

Second International Workshop on Multiple Endocrine Neoplasia Type 2 (MEN 2), Cambridge, 17 to 20 September 1986
B Ponder and E D Williams
J Med Genet 1987; 24: 507-508. doi:10.1136/jmg.24.8.507 [PDF] [Request Permissions]

Research Article

Adult polycystic kidney disease.
R Harris
J Med Genet 1987; 24: 449-450. doi:10.1136/jmg.24.8.449 [PDF] [Request Permissions]

Molecular genetics of human chromosome 16.
G R Sutherland, S Reeders, V J Hyland, D F Callen, A Fratini, and J C Mulley
J Med Genet 1987; 24: 451-456. doi:10.1136/jmg.24.8.451 [Abstract] [PDF] [Request Permissions]

Studies of genetic linkage between adult polycystic kidney disease and three markers on chromosome 16.
M L Watson, A F Wright, A M Macnicol, P L Allan, J F Clayton, M Dempster, S J Jeremiah, G Corney, and D A Hopkinson
J Med Genet 1987; 24: 457-461. doi:10.1136/jmg.24.8.457 [Abstract] [PDF] [Request Permissions]

Localisation of a mutation producing autosomal dominant polycystic kidney disease without renal failure.
M Ryynanen, M M Dolata, E Lampainen, and S T Reeders
J Med Genet 1987; 24: 462-465. doi:10.1136/jmg.24.8.462 [Abstract] [PDF] [Request Permissions]

Adult polycystic kidney disease and linked RFLPs at the alpha globin locus: a genetic study in the South Wales population.
L P Lazarou, F Davies, M Sarfarazi, G A Coles, and P S Harper
J Med Genet 1987; 24: 466-473. doi:10.1136/jmg.24.8.466 [Abstract] [PDF] [Request Permissions]

Polycystic kidney disease in children: a genetic and epidemiological study of 82 Finnish patients.
H Kääriäinen
J Med Genet 1987; 24: 474-481. doi:10.1136/jmg.24.8.474 [Abstract] [PDF] [Request Permissions]

Trends in pyloric stenosis incidence, Atlanta, 1968 to 1982.
E J Lammer and L D Edmonds
J Med Genet 1987; 24: 482-487. doi:10.1136/jmg.24.8.482 [Abstract] [PDF] [Request Permissions]

Intrafamilial variation in Cohen syndrome.
I D Young and J R Moore
J Med Genet 1987; 24: 488-492. doi:10.1136/jmg.24.8.488 [Abstract] [PDF] [Request Permissions]

Congenital scalp defects with distal limb reduction anomalies.
J P Fryns
J Med Genet 1987; 24: 493-496. doi:10.1136/jmg.24.8.493 [PDF] [Request Permissions]

A chromosome supplement to the London Dysmorphology Database.
J Brandl and T Grimm
J Med Genet 1987; 24: 497-498. doi:10.1136/jmg.24.8.497 [Abstract] [PDF] [Request Permissions]

Detection of centromeric regions of chromosomes by immunofluorescence: procedure and application.
M K Oaks, D P O'Malley, J R Kateley, and W E Maldonado
J Med Genet 1987; 24: 498-499. doi:10.1136/jmg.24.8.498 [PDF] [Request Permissions]

Trisomy 13 in monozygotic twins discordant for major congenital anomalies.
N Naor, Y Amir, T Cohen, and S Davidson
J Med Genet 1987; 24: 500-502. doi:10.1136/jmg.24.8.500 [Abstract] [PDF] [Request Permissions]

Partial trisomy 17q and a generalised bone dysplasia in a 12 week fetus.
A Robb, L Forsyth, and J Tolmie
J Med Genet 1987; 24: 502-504. doi:10.1136/jmg.24.8.502 [Abstract] [PDF] [Request Permissions]

The London Dysmorphology Database.
R M Winter and M Baraitser
J Med Genet 1987; 24: 509-510. doi:10.1136/jmg.24.8.509 [PDF] [Request Permissions]

Pericentric inversion and sterility.
A Barros, M C Tavares, M P Gomes, and M P Tavares
J Med Genet 1987; 24: 510. doi:10.1136/jmg.24.8.510 [PDF] [Request Permissions]

The craniocardioskeletal syndrome and the Noonan-like short stature syndrome are possibly the same entity.
J Sánchez Corona and J M Cantú
J Med Genet 1987; 24: 510-511. doi:10.1136/jmg.24.8.510-a [PDF] [Request Permissions]

Mental retardation with blepharophimosis.
B Say and N Barber
J Med Genet 1987; 24: 511. doi:10.1136/jmg.24.8.511-a [PDF] [Request Permissions]

Register for free content

The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.

Genetics jobs

Show me all >>

	Correspondence Michael Baraitser and Michael A Patton J Med Genet 1987; 24: 511. doi:10.1136/jmg.24.8.511 [PDF] [Request Permissions]

	The Second Manchester Birth Defects Conference, 1 to 3 October 1986 John Burn J Med Genet 1987; 24: 505-507. doi:10.1136/jmg.24.8.505 [PDF] [Request Permissions]

	Second International Workshop on Multiple Endocrine Neoplasia Type 2 (MEN 2), Cambridge, 17 to 20 September 1986 B Ponder and E D Williams J Med Genet 1987; 24: 507-508. doi:10.1136/jmg.24.8.507 [PDF] [Request Permissions]

	Adult polycystic kidney disease. R Harris J Med Genet 1987; 24: 449-450. doi:10.1136/jmg.24.8.449 [PDF] [Request Permissions]

	Molecular genetics of human chromosome 16. G R Sutherland, S Reeders, V J Hyland, D F Callen, A Fratini, and J C Mulley J Med Genet 1987; 24: 451-456. doi:10.1136/jmg.24.8.451 [Abstract] [PDF] [Request Permissions]

	Studies of genetic linkage between adult polycystic kidney disease and three markers on chromosome 16. M L Watson, A F Wright, A M Macnicol, P L Allan, J F Clayton, M Dempster, S J Jeremiah, G Corney, and D A Hopkinson J Med Genet 1987; 24: 457-461. doi:10.1136/jmg.24.8.457 [Abstract] [PDF] [Request Permissions]

	Localisation of a mutation producing autosomal dominant polycystic kidney disease without renal failure. M Ryynanen, M M Dolata, E Lampainen, and S T Reeders J Med Genet 1987; 24: 462-465. doi:10.1136/jmg.24.8.462 [Abstract] [PDF] [Request Permissions]

	Adult polycystic kidney disease and linked RFLPs at the alpha globin locus: a genetic study in the South Wales population. L P Lazarou, F Davies, M Sarfarazi, G A Coles, and P S Harper J Med Genet 1987; 24: 466-473. doi:10.1136/jmg.24.8.466 [Abstract] [PDF] [Request Permissions]

	Polycystic kidney disease in children: a genetic and epidemiological study of 82 Finnish patients. H Kääriäinen J Med Genet 1987; 24: 474-481. doi:10.1136/jmg.24.8.474 [Abstract] [PDF] [Request Permissions]

	Trends in pyloric stenosis incidence, Atlanta, 1968 to 1982. E J Lammer and L D Edmonds J Med Genet 1987; 24: 482-487. doi:10.1136/jmg.24.8.482 [Abstract] [PDF] [Request Permissions]

	Intrafamilial variation in Cohen syndrome. I D Young and J R Moore J Med Genet 1987; 24: 488-492. doi:10.1136/jmg.24.8.488 [Abstract] [PDF] [Request Permissions]

	Congenital scalp defects with distal limb reduction anomalies. J P Fryns J Med Genet 1987; 24: 493-496. doi:10.1136/jmg.24.8.493 [PDF] [Request Permissions]

	A chromosome supplement to the London Dysmorphology Database. J Brandl and T Grimm J Med Genet 1987; 24: 497-498. doi:10.1136/jmg.24.8.497 [Abstract] [PDF] [Request Permissions]

	Detection of centromeric regions of chromosomes by immunofluorescence: procedure and application. M K Oaks, D P O'Malley, J R Kateley, and W E Maldonado J Med Genet 1987; 24: 498-499. doi:10.1136/jmg.24.8.498 [PDF] [Request Permissions]

	Trisomy 13 in monozygotic twins discordant for major congenital anomalies. N Naor, Y Amir, T Cohen, and S Davidson J Med Genet 1987; 24: 500-502. doi:10.1136/jmg.24.8.500 [Abstract] [PDF] [Request Permissions]

	Partial trisomy 17q and a generalised bone dysplasia in a 12 week fetus. A Robb, L Forsyth, and J Tolmie J Med Genet 1987; 24: 502-504. doi:10.1136/jmg.24.8.502 [Abstract] [PDF] [Request Permissions]

	The London Dysmorphology Database. R M Winter and M Baraitser J Med Genet 1987; 24: 509-510. doi:10.1136/jmg.24.8.509 [PDF] [Request Permissions]

	Pericentric inversion and sterility. A Barros, M C Tavares, M P Gomes, and M P Tavares J Med Genet 1987; 24: 510. doi:10.1136/jmg.24.8.510 [PDF] [Request Permissions]

	The craniocardioskeletal syndrome and the Noonan-like short stature syndrome are possibly the same entity. J Sánchez Corona and J M Cantú J Med Genet 1987; 24: 510-511. doi:10.1136/jmg.24.8.510-a [PDF] [Request Permissions]

	Mental retardation with blepharophimosis. B Say and N Barber J Med Genet 1987; 24: 511. doi:10.1136/jmg.24.8.511-a [PDF] [Request Permissions]