J Med Genet -- Table of Contents (24 [11])

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November 1987 (Volume 24, Number 11). [Index by author]

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Articles

Editorial note
Peter S Harper
J Med Genet 1987; 24: 713. doi:10.1136/jmg.24.11.713 [PDF] [Request Permissions]

Book Reviews

A Dictionary of Genetic Engineering
K Temple and S Malcolm
J Med Genet 1987; 24: 717. doi:10.1136/jmg.24.11.717 [PDF] [Request Permissions]

Genetics and the Law III
Thaddeus E Kelly
J Med Genet 1987; 24: 717. doi:10.1136/jmg.24.11.717-a [PDF] [Request Permissions]

The Genetics of the Skeleton
Ruth Wynne-Davies
J Med Genet 1987; 24: 717-718. doi:10.1136/jmg.24.11.717-b [PDF] [Request Permissions]

Craniostenosis: Diagnosis, Evaluation, and Management
H E Hughes
J Med Genet 1987; 24: 718. doi:10.1136/jmg.24.11.718 [PDF] [Request Permissions]

Cell and Molecular Biology of the Cytoskeleton
P N Goodfellow
J Med Genet 1987; 24: 718-719. doi:10.1136/jmg.24.11.718-a [PDF] [Request Permissions]

Mendelian Inheritance in Man
Peter S Harper
J Med Genet 1987; 24: 719. doi:10.1136/jmg.24.11.719 [PDF] [Request Permissions]

Biochemistry and Biology of Plasma Lipoproteins
Alan Rees
J Med Genet 1987; 24: 719-720. doi:10.1136/jmg.24.11.719-a [PDF] [Request Permissions]

Chorionic Villi Sampling
Bernadette Modell
J Med Genet 1987; 24: 720. doi:10.1136/jmg.24.11.720 [PDF] [Request Permissions]

Research Article

The molecular genetics of human chromosome 6.
V Cunliffe and J Trowsdale
J Med Genet 1987; 24: 649-658. doi:10.1136/jmg.24.11.649 [Abstract] [PDF] [Request Permissions]

Hypohidrotic ectodermal dysplasia.
A Clarke
J Med Genet 1987; 24: 659-663. doi:10.1136/jmg.24.11.659 [PDF] [Request Permissions]

Malignant melanoma in families of children with osteosarcoma, chondrosarcoma, and adrenal cortical carcinoma.
A L Hartley, J M Birch, H B Marsden, and M Harris
J Med Genet 1987; 24: 664-668. doi:10.1136/jmg.24.11.664 [Abstract] [PDF] [Request Permissions]

Variant forms of ataxia telangiectasia.
A M Taylor, E Flude, B Laher, M Stacey, E McKay, J Watt, S H Green, and A E Harding
J Med Genet 1987; 24: 669-677. doi:10.1136/jmg.24.11.669 [Abstract] [PDF] [Request Permissions]

The inheritance of fragile sites: apparent absence of fra(2)(q13) in the parents of three unrelated probands.
L Keskiaho, S Knuutila, H Pihko, A Nuutila, U Kaski, M Koivikko, and A de la Chapelle
J Med Genet 1987; 24: 678-683. doi:10.1136/jmg.24.11.678 [Abstract] [PDF] [Request Permissions]

Familial t(8;15)(p23.3;q22.3): report of two cases with dup(15) (q22.3----qter).
D J Goldstein, R E Ward, W C Nichols, and C G Palmer
J Med Genet 1987; 24: 684-687. doi:10.1136/jmg.24.11.684 [Abstract] [PDF] [Request Permissions]

Congenital anal anomalies in two families with the Opitz G syndrome.
J L Tolmie, N Coutts, and I K Drainer
J Med Genet 1987; 24: 688-691. doi:10.1136/jmg.24.11.688 [Abstract] [PDF] [Request Permissions]

Fetal valproate syndrome: is there a recognisable phenotype?
R M Winter, D Donnai, J Burn, and S M Tucker
J Med Genet 1987; 24: 692-695. doi:10.1136/jmg.24.11.692 [Abstract] [PDF] [Request Permissions]

Deletion (13)(q13q14.3) with retinoblastoma: confirmation and extension of a recognisable pattern of clinical features in retinoblastoma patients with 13q deletion.
T Motegi, K Ikeda, K Watanabe, Y Yanagawa, and K Minoda
J Med Genet 1987; 24: 696-697. doi:10.1136/jmg.24.11.696 [Abstract] [PDF] [Request Permissions]

The clinical features of Ehlers-Danlos syndrome type VII due to a deletion of 24 amino acids from the pro alpha 1(I) chain of type I procollagen.
W G Cole, R Evans, and D O Sillence
J Med Genet 1987; 24: 698-701. doi:10.1136/jmg.24.11.698 [Abstract] [PDF] [Request Permissions]

Spastic paraplegia associated with brachydactyly and cone shaped epiphyses.
J S Fitzsimmons and P R Guilbert
J Med Genet 1987; 24: 702-705. doi:10.1136/jmg.24.11.702 [Abstract] [PDF] [Request Permissions]

Partial deletion 21: case report with biochemical studies and review.
N J Carpenter, J S Mayes, B Say, and D P Wilson
J Med Genet 1987; 24: 706-709. doi:10.1136/jmg.24.11.706 [Abstract] [PDF] [Request Permissions]

Deletion 15q21.1----q22.1 resulting from a paternal insertion into chromosome 5.
M Y Yip, M Selikowitz, N Don, A Kovacic, S Purvis-Smith, and P R Lam-Po-Tang
J Med Genet 1987; 24: 709-712. doi:10.1136/jmg.24.11.709 [Abstract] [PDF] [Request Permissions]

Unknown syndrome: holoprosencephaly, congenital heart defects, and polydactyly.
I D Young and D J Madders
J Med Genet 1987; 24: 714-715. doi:10.1136/jmg.24.11.714 [Abstract] [PDF] [Request Permissions]

Unknown syndrome: abnormal facies, congenital heart defects, hypothyroidism, and severe retardation.
I D Young and K Simpson
J Med Genet 1987; 24: 715-716. doi:10.1136/jmg.24.11.715 [Abstract] [PDF] [Request Permissions]

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	Editorial note Peter S Harper J Med Genet 1987; 24: 713. doi:10.1136/jmg.24.11.713 [PDF] [Request Permissions]

	A Dictionary of Genetic Engineering K Temple and S Malcolm J Med Genet 1987; 24: 717. doi:10.1136/jmg.24.11.717 [PDF] [Request Permissions]

	Genetics and the Law III Thaddeus E Kelly J Med Genet 1987; 24: 717. doi:10.1136/jmg.24.11.717-a [PDF] [Request Permissions]

	The Genetics of the Skeleton Ruth Wynne-Davies J Med Genet 1987; 24: 717-718. doi:10.1136/jmg.24.11.717-b [PDF] [Request Permissions]

	Craniostenosis: Diagnosis, Evaluation, and Management H E Hughes J Med Genet 1987; 24: 718. doi:10.1136/jmg.24.11.718 [PDF] [Request Permissions]

	Cell and Molecular Biology of the Cytoskeleton P N Goodfellow J Med Genet 1987; 24: 718-719. doi:10.1136/jmg.24.11.718-a [PDF] [Request Permissions]

	Mendelian Inheritance in Man Peter S Harper J Med Genet 1987; 24: 719. doi:10.1136/jmg.24.11.719 [PDF] [Request Permissions]

	Biochemistry and Biology of Plasma Lipoproteins Alan Rees J Med Genet 1987; 24: 719-720. doi:10.1136/jmg.24.11.719-a [PDF] [Request Permissions]

	Chorionic Villi Sampling Bernadette Modell J Med Genet 1987; 24: 720. doi:10.1136/jmg.24.11.720 [PDF] [Request Permissions]

	The molecular genetics of human chromosome 6. V Cunliffe and J Trowsdale J Med Genet 1987; 24: 649-658. doi:10.1136/jmg.24.11.649 [Abstract] [PDF] [Request Permissions]

	Hypohidrotic ectodermal dysplasia. A Clarke J Med Genet 1987; 24: 659-663. doi:10.1136/jmg.24.11.659 [PDF] [Request Permissions]

	Malignant melanoma in families of children with osteosarcoma, chondrosarcoma, and adrenal cortical carcinoma. A L Hartley, J M Birch, H B Marsden, and M Harris J Med Genet 1987; 24: 664-668. doi:10.1136/jmg.24.11.664 [Abstract] [PDF] [Request Permissions]

	Variant forms of ataxia telangiectasia. A M Taylor, E Flude, B Laher, M Stacey, E McKay, J Watt, S H Green, and A E Harding J Med Genet 1987; 24: 669-677. doi:10.1136/jmg.24.11.669 [Abstract] [PDF] [Request Permissions]

	The inheritance of fragile sites: apparent absence of fra(2)(q13) in the parents of three unrelated probands. L Keskiaho, S Knuutila, H Pihko, A Nuutila, U Kaski, M Koivikko, and A de la Chapelle J Med Genet 1987; 24: 678-683. doi:10.1136/jmg.24.11.678 [Abstract] [PDF] [Request Permissions]

	Familial t(8;15)(p23.3;q22.3): report of two cases with dup(15) (q22.3----qter). D J Goldstein, R E Ward, W C Nichols, and C G Palmer J Med Genet 1987; 24: 684-687. doi:10.1136/jmg.24.11.684 [Abstract] [PDF] [Request Permissions]

	Congenital anal anomalies in two families with the Opitz G syndrome. J L Tolmie, N Coutts, and I K Drainer J Med Genet 1987; 24: 688-691. doi:10.1136/jmg.24.11.688 [Abstract] [PDF] [Request Permissions]

	Fetal valproate syndrome: is there a recognisable phenotype? R M Winter, D Donnai, J Burn, and S M Tucker J Med Genet 1987; 24: 692-695. doi:10.1136/jmg.24.11.692 [Abstract] [PDF] [Request Permissions]

	Deletion (13)(q13q14.3) with retinoblastoma: confirmation and extension of a recognisable pattern of clinical features in retinoblastoma patients with 13q deletion. T Motegi, K Ikeda, K Watanabe, Y Yanagawa, and K Minoda J Med Genet 1987; 24: 696-697. doi:10.1136/jmg.24.11.696 [Abstract] [PDF] [Request Permissions]

	The clinical features of Ehlers-Danlos syndrome type VII due to a deletion of 24 amino acids from the pro alpha 1(I) chain of type I procollagen. W G Cole, R Evans, and D O Sillence J Med Genet 1987; 24: 698-701. doi:10.1136/jmg.24.11.698 [Abstract] [PDF] [Request Permissions]

	Spastic paraplegia associated with brachydactyly and cone shaped epiphyses. J S Fitzsimmons and P R Guilbert J Med Genet 1987; 24: 702-705. doi:10.1136/jmg.24.11.702 [Abstract] [PDF] [Request Permissions]

	Partial deletion 21: case report with biochemical studies and review. N J Carpenter, J S Mayes, B Say, and D P Wilson J Med Genet 1987; 24: 706-709. doi:10.1136/jmg.24.11.706 [Abstract] [PDF] [Request Permissions]

	Deletion 15q21.1----q22.1 resulting from a paternal insertion into chromosome 5. M Y Yip, M Selikowitz, N Don, A Kovacic, S Purvis-Smith, and P R Lam-Po-Tang J Med Genet 1987; 24: 709-712. doi:10.1136/jmg.24.11.709 [Abstract] [PDF] [Request Permissions]

	Unknown syndrome: holoprosencephaly, congenital heart defects, and polydactyly. I D Young and D J Madders J Med Genet 1987; 24: 714-715. doi:10.1136/jmg.24.11.714 [Abstract] [PDF] [Request Permissions]

	Unknown syndrome: abnormal facies, congenital heart defects, hypothyroidism, and severe retardation. I D Young and K Simpson J Med Genet 1987; 24: 715-716. doi:10.1136/jmg.24.11.715 [Abstract] [PDF] [Request Permissions]