J Med Genet -- Table of Contents (25 [7])

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July 1988 (Volume 25, Number 7). [Index by author]

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Articles

Editorial
Robin Winter and Dian Donnai
J Med Genet 1988; 25: 433. doi:10.1136/jmg.25.7.433 [PDF] [Request Permissions]

Research Article

The value of the study of natural history in genetic disorders and congenital anomaly syndromes.
J G Hall
J Med Genet 1988; 25: 434-444. doi:10.1136/jmg.25.7.434 [Abstract] [PDF] [Request Permissions]

Use of computers in dysmorphology.
J H Diliberti
J Med Genet 1988; 25: 445-453. doi:10.1136/jmg.25.7.445 [Abstract] [PDF] [Request Permissions]

Microdeletion syndromes, balanced translocations, and gene mapping.
A Schinzel
J Med Genet 1988; 25: 454-462. doi:10.1136/jmg.25.7.454 [Abstract] [PDF] [Request Permissions]

Dysmorphic syndromes with demonstrable biochemical abnormalities.
P T Clayton and E Thompson
J Med Genet 1988; 25: 463-472. doi:10.1136/jmg.25.7.463 [Abstract] [PDF] [Request Permissions]

Molecular approaches to dysmorphology.
A Ivens, G Moore, and R Williamson
J Med Genet 1988; 25: 473-479. doi:10.1136/jmg.25.7.473 [Abstract] [PDF] [Request Permissions]

Malformation syndromes: a review of mouse/human homology.
R M Winter
J Med Genet 1988; 25: 480-487. doi:10.1136/jmg.25.7.480 [Abstract] [PDF] [Request Permissions]

Pseudoxanthoma elasticum (Grönblad-Strandberg syndrome).
D Viljoen
J Med Genet 1988; 25: 488-490. doi:10.1136/jmg.25.7.488 [PDF] [Request Permissions]

Auralcephalosyndactyly: a new hereditary craniosynostosis syndrome.
T W Kurczynski and S M Casperson
J Med Genet 1988; 25: 491-493. doi:10.1136/jmg.25.7.491 [Abstract] [PDF] [Request Permissions]

Unknown syndrome: Hirschsprung's disease, microcephaly, and iris coloboma: a new syndrome of defective neuronal migration.
J A Hurst, M Markiewicz, D Kumar, and E M Brett
J Med Genet 1988; 25: 494-497. doi:10.1136/jmg.25.7.494 [Abstract] [PDF] [Request Permissions]

Unknown syndrome: abnormal facies, hypothyroidism, and severe retardation: a second patient.
J P Fryns and P Moerman
J Med Genet 1988; 25: 498-499. doi:10.1136/jmg.25.7.498 [Abstract] [PDF] [Request Permissions]

A further patient with the lethal type of Larsen syndrome.
J Clayton-Smith and D Donnai
J Med Genet 1988; 25: 499-500. doi:10.1136/jmg.25.7.499 [Abstract] [PDF] [Request Permissions]

Holoprosencephaly and postaxial polydactyly: another observation.
P Moerman and J P Fryns
J Med Genet 1988; 25: 501-502. doi:10.1136/jmg.25.7.501 [PDF] [Request Permissions]

Holoprosencephaly, ventricular septal defect, and postaxial polydactyly in a human embryo.
K Shiota and T Tanimura
J Med Genet 1988; 25: 502-503. doi:10.1136/jmg.25.7.502 [PDF] [Request Permissions]

Syndactyly, ectodermal dysplasia, and cleft lip and palate.
J Zlotogora and G Ogur
J Med Genet 1988; 25: 503. doi:10.1136/jmg.25.7.503 [PDF] [Request Permissions]

Are 'upper' and 'lower' neural tube defects aetiologically different?
M F Frecker, F C Fraser, and W D Heneghan
J Med Genet 1988; 25: 503-504. doi:10.1136/jmg.25.7.503-a [PDF] [Request Permissions]

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	Editorial Robin Winter and Dian Donnai J Med Genet 1988; 25: 433. doi:10.1136/jmg.25.7.433 [PDF] [Request Permissions]

	The value of the study of natural history in genetic disorders and congenital anomaly syndromes. J G Hall J Med Genet 1988; 25: 434-444. doi:10.1136/jmg.25.7.434 [Abstract] [PDF] [Request Permissions]

	Use of computers in dysmorphology. J H Diliberti J Med Genet 1988; 25: 445-453. doi:10.1136/jmg.25.7.445 [Abstract] [PDF] [Request Permissions]

	Microdeletion syndromes, balanced translocations, and gene mapping. A Schinzel J Med Genet 1988; 25: 454-462. doi:10.1136/jmg.25.7.454 [Abstract] [PDF] [Request Permissions]

	Dysmorphic syndromes with demonstrable biochemical abnormalities. P T Clayton and E Thompson J Med Genet 1988; 25: 463-472. doi:10.1136/jmg.25.7.463 [Abstract] [PDF] [Request Permissions]

	Molecular approaches to dysmorphology. A Ivens, G Moore, and R Williamson J Med Genet 1988; 25: 473-479. doi:10.1136/jmg.25.7.473 [Abstract] [PDF] [Request Permissions]

	Malformation syndromes: a review of mouse/human homology. R M Winter J Med Genet 1988; 25: 480-487. doi:10.1136/jmg.25.7.480 [Abstract] [PDF] [Request Permissions]

	Pseudoxanthoma elasticum (Grönblad-Strandberg syndrome). D Viljoen J Med Genet 1988; 25: 488-490. doi:10.1136/jmg.25.7.488 [PDF] [Request Permissions]

	Auralcephalosyndactyly: a new hereditary craniosynostosis syndrome. T W Kurczynski and S M Casperson J Med Genet 1988; 25: 491-493. doi:10.1136/jmg.25.7.491 [Abstract] [PDF] [Request Permissions]

	Unknown syndrome: Hirschsprung's disease, microcephaly, and iris coloboma: a new syndrome of defective neuronal migration. J A Hurst, M Markiewicz, D Kumar, and E M Brett J Med Genet 1988; 25: 494-497. doi:10.1136/jmg.25.7.494 [Abstract] [PDF] [Request Permissions]

	Unknown syndrome: abnormal facies, hypothyroidism, and severe retardation: a second patient. J P Fryns and P Moerman J Med Genet 1988; 25: 498-499. doi:10.1136/jmg.25.7.498 [Abstract] [PDF] [Request Permissions]

	A further patient with the lethal type of Larsen syndrome. J Clayton-Smith and D Donnai J Med Genet 1988; 25: 499-500. doi:10.1136/jmg.25.7.499 [Abstract] [PDF] [Request Permissions]

	Holoprosencephaly and postaxial polydactyly: another observation. P Moerman and J P Fryns J Med Genet 1988; 25: 501-502. doi:10.1136/jmg.25.7.501 [PDF] [Request Permissions]

	Holoprosencephaly, ventricular septal defect, and postaxial polydactyly in a human embryo. K Shiota and T Tanimura J Med Genet 1988; 25: 502-503. doi:10.1136/jmg.25.7.502 [PDF] [Request Permissions]

	Syndactyly, ectodermal dysplasia, and cleft lip and palate. J Zlotogora and G Ogur J Med Genet 1988; 25: 503. doi:10.1136/jmg.25.7.503 [PDF] [Request Permissions]

	Are 'upper' and 'lower' neural tube defects aetiologically different? M F Frecker, F C Fraser, and W D Heneghan J Med Genet 1988; 25: 503-504. doi:10.1136/jmg.25.7.503-a [PDF] [Request Permissions]