J Med Genet -- Table of Contents (24 [7])

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July 1987 (Volume 24, Number 7). [Index by author]

		Articles Obituaries Articles Book Reviews Research Article

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Articles

Editorial
Peter S Harper
J Med Genet 1987; 24: 385. doi:10.1136/jmg.24.7.385 [PDF] [Request Permissions]

Obituaries

Dr John Alexander Fraser Roberts, CBE, FRS, MA, DSc, MD, FRCP, FRCPsych
Marcus E Pembrey
J Med Genet 1987; 24: 442-444. doi:10.1136/jmg.24.7.442 [PDF] [Request Permissions]

Articles

Editorial
Peter S Harper
J Med Genet 1987; 24: 385. doi:10.1136/jmg.24.7.385 [PDF] [Request Permissions]

Book Reviews

Goldberg's Genetic and Metabolic Eye Disease
Barrie Jay
J Med Genet 1987; 24: 445. doi:10.1136/jmg.24.7.445 [PDF] [Request Permissions]

Human Prenatal Diagnosis
D J H Brock
J Med Genet 1987; 24: 445. doi:10.1136/jmg.24.7.445-a [PDF] [Request Permissions]

Oncogenes: Their Role in Normal and Malignant Growth
D G Harnden
J Med Genet 1987; 24: 445-446. doi:10.1136/jmg.24.7.445-b [PDF] [Request Permissions]

Genetics of Man
R F Mueller
J Med Genet 1987; 24: 446. doi:10.1136/jmg.24.7.446 [PDF] [Request Permissions]

Human Growth: A Multidisciplinary Review
I A Hughes
J Med Genet 1987; 24: 446-447. doi:10.1136/jmg.24.7.446-a [PDF] [Request Permissions]

Human Chromosomes. Structure, Behaviour, Effects
P Cooke
J Med Genet 1987; 24: 447. doi:10.1136/jmg.24.7.447 [PDF] [Request Permissions]

Human Cytogenetics: A Practical Approach
Selwyn Roberts
J Med Genet 1987; 24: 447-448. doi:10.1136/jmg.24.7.447-a [PDF] [Request Permissions]

Leukemia: Recent Advances in Biology and Treatment
N G Testa
J Med Genet 1987; 24: 448. doi:10.1136/jmg.24.7.448 [PDF] [Request Permissions]

Research Article

Osteogenesis imperfecta type IIA: evidence for dominant inheritance.
I D Young, E M Thompson, C M Hall, and M E Pembrey
J Med Genet 1987; 24: 386-389. doi:10.1136/jmg.24.7.386 [Abstract] [PDF] [Request Permissions]

Recurrence risks and prognosis in severe sporadic osteogenesis imperfecta.
E M Thompson, I D Young, C M Hall, and M E Pembrey
J Med Genet 1987; 24: 390-405. doi:10.1136/jmg.24.7.390 [Abstract] [PDF] [Request Permissions]

Prenatal prediction of osteogenesis imperfecta (OI type IV): exclusion of inheritance using a collagen gene probe.
P Tsipouras, R C Schwartz, J D Goldberg, R L Berkowitz, and F Ramirez
J Med Genet 1987; 24: 406-409. doi:10.1136/jmg.24.7.406 [Abstract] [PDF] [Request Permissions]

Wolf-Hirschhorn locus is distal to D4S10 on short arm of chromosome 4.
C McKeown, A P Read, A Dodge, O Stecko, A Mercer, and R Harris
J Med Genet 1987; 24: 410-412. doi:10.1136/jmg.24.7.410 [Abstract] [PDF] [Request Permissions]

The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.
H Veenema, N J Carpenter, E Bakker, M H Hofker, A M Ward, and P L Pearson
J Med Genet 1987; 24: 413-421. doi:10.1136/jmg.24.7.413 [Abstract] [PDF] [Request Permissions]

Postaxial acrofacial dysostosis (Miller) syndrome.
D Donnai, H E Hughes, and R M Winter
J Med Genet 1987; 24: 422-425. doi:10.1136/jmg.24.7.422 [PDF] [Request Permissions]

18q-syndrome and extraskeletal Ewing's sarcoma.
M Machin Valtueña, J M Garcia-Sagredo, A Muñoz Villa, C Lozano Giménez, and J M Aparicio Meix
J Med Genet 1987; 24: 426-428. doi:10.1136/jmg.24.7.426 [Abstract] [PDF] [Request Permissions]

An isodicentric X chromosome with short arm fusion in a woman without somatic features of Turner's syndrome.
I C Barnes, D J Curtis, and S L Duncan
J Med Genet 1987; 24: 428-431. doi:10.1136/jmg.24.7.428 [Abstract] [PDF] [Request Permissions]

Translocation X;13 in a patient with retinoblastoma.
G Ponzio, E Savin, G Cattaneo, M P Ghiotti, A Marra, O Zuffardi, and C Danesino
J Med Genet 1987; 24: 431-434. doi:10.1136/jmg.24.7.431 [Abstract] [PDF] [Request Permissions]

Partial monosomy 12p13.1----13.3.
D R Romain, J Goldsmith, L M Columbano-Green, C J Chapman, R H Smythe, and R G Parfitt
J Med Genet 1987; 24: 434-436. doi:10.1136/jmg.24.7.434 [Abstract] [PDF] [Request Permissions]

De novo 2q+ masquerading as Smith-Lemli-Opitz syndrome.
A E Donnenfeld, E H Zackai, D M McDonald, R Aquino, and B S Emanuel
J Med Genet 1987; 24: 436-439. doi:10.1136/jmg.24.7.436 [Abstract] [PDF] [Request Permissions]

Incontinentia pigmenti in a boy with Klinefelter's syndrome.
A D Ormerod, M I White, E McKay, and A W Johnston
J Med Genet 1987; 24: 439-441. doi:10.1136/jmg.24.7.439 [Abstract] [PDF] [Request Permissions]

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	Editorial Peter S Harper J Med Genet 1987; 24: 385. doi:10.1136/jmg.24.7.385 [PDF] [Request Permissions]

	Dr John Alexander Fraser Roberts, CBE, FRS, MA, DSc, MD, FRCP, FRCPsych Marcus E Pembrey J Med Genet 1987; 24: 442-444. doi:10.1136/jmg.24.7.442 [PDF] [Request Permissions]

	Goldberg's Genetic and Metabolic Eye Disease Barrie Jay J Med Genet 1987; 24: 445. doi:10.1136/jmg.24.7.445 [PDF] [Request Permissions]

	Human Prenatal Diagnosis D J H Brock J Med Genet 1987; 24: 445. doi:10.1136/jmg.24.7.445-a [PDF] [Request Permissions]

	Oncogenes: Their Role in Normal and Malignant Growth D G Harnden J Med Genet 1987; 24: 445-446. doi:10.1136/jmg.24.7.445-b [PDF] [Request Permissions]

	Genetics of Man R F Mueller J Med Genet 1987; 24: 446. doi:10.1136/jmg.24.7.446 [PDF] [Request Permissions]

	Human Growth: A Multidisciplinary Review I A Hughes J Med Genet 1987; 24: 446-447. doi:10.1136/jmg.24.7.446-a [PDF] [Request Permissions]

	Human Chromosomes. Structure, Behaviour, Effects P Cooke J Med Genet 1987; 24: 447. doi:10.1136/jmg.24.7.447 [PDF] [Request Permissions]

	Human Cytogenetics: A Practical Approach Selwyn Roberts J Med Genet 1987; 24: 447-448. doi:10.1136/jmg.24.7.447-a [PDF] [Request Permissions]

	Leukemia: Recent Advances in Biology and Treatment N G Testa J Med Genet 1987; 24: 448. doi:10.1136/jmg.24.7.448 [PDF] [Request Permissions]

	Osteogenesis imperfecta type IIA: evidence for dominant inheritance. I D Young, E M Thompson, C M Hall, and M E Pembrey J Med Genet 1987; 24: 386-389. doi:10.1136/jmg.24.7.386 [Abstract] [PDF] [Request Permissions]

	Recurrence risks and prognosis in severe sporadic osteogenesis imperfecta. E M Thompson, I D Young, C M Hall, and M E Pembrey J Med Genet 1987; 24: 390-405. doi:10.1136/jmg.24.7.390 [Abstract] [PDF] [Request Permissions]

	Prenatal prediction of osteogenesis imperfecta (OI type IV): exclusion of inheritance using a collagen gene probe. P Tsipouras, R C Schwartz, J D Goldberg, R L Berkowitz, and F Ramirez J Med Genet 1987; 24: 406-409. doi:10.1136/jmg.24.7.406 [Abstract] [PDF] [Request Permissions]

	Wolf-Hirschhorn locus is distal to D4S10 on short arm of chromosome 4. C McKeown, A P Read, A Dodge, O Stecko, A Mercer, and R Harris J Med Genet 1987; 24: 410-412. doi:10.1136/jmg.24.7.410 [Abstract] [PDF] [Request Permissions]

	The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27. H Veenema, N J Carpenter, E Bakker, M H Hofker, A M Ward, and P L Pearson J Med Genet 1987; 24: 413-421. doi:10.1136/jmg.24.7.413 [Abstract] [PDF] [Request Permissions]

	Postaxial acrofacial dysostosis (Miller) syndrome. D Donnai, H E Hughes, and R M Winter J Med Genet 1987; 24: 422-425. doi:10.1136/jmg.24.7.422 [PDF] [Request Permissions]

	18q-syndrome and extraskeletal Ewing's sarcoma. M Machin Valtueña, J M Garcia-Sagredo, A Muñoz Villa, C Lozano Giménez, and J M Aparicio Meix J Med Genet 1987; 24: 426-428. doi:10.1136/jmg.24.7.426 [Abstract] [PDF] [Request Permissions]

	An isodicentric X chromosome with short arm fusion in a woman without somatic features of Turner's syndrome. I C Barnes, D J Curtis, and S L Duncan J Med Genet 1987; 24: 428-431. doi:10.1136/jmg.24.7.428 [Abstract] [PDF] [Request Permissions]

	Translocation X;13 in a patient with retinoblastoma. G Ponzio, E Savin, G Cattaneo, M P Ghiotti, A Marra, O Zuffardi, and C Danesino J Med Genet 1987; 24: 431-434. doi:10.1136/jmg.24.7.431 [Abstract] [PDF] [Request Permissions]

	Partial monosomy 12p13.1----13.3. D R Romain, J Goldsmith, L M Columbano-Green, C J Chapman, R H Smythe, and R G Parfitt J Med Genet 1987; 24: 434-436. doi:10.1136/jmg.24.7.434 [Abstract] [PDF] [Request Permissions]

	De novo 2q+ masquerading as Smith-Lemli-Opitz syndrome. A E Donnenfeld, E H Zackai, D M McDonald, R Aquino, and B S Emanuel J Med Genet 1987; 24: 436-439. doi:10.1136/jmg.24.7.436 [Abstract] [PDF] [Request Permissions]

	Incontinentia pigmenti in a boy with Klinefelter's syndrome. A D Ormerod, M I White, E McKay, and A W Johnston J Med Genet 1987; 24: 439-441. doi:10.1136/jmg.24.7.439 [Abstract] [PDF] [Request Permissions]