J Med Genet -- Table of Contents (17 [2])

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April 1980 (Volume 17, Number 2). [Index by author]

		Articles Correspondence Articles Book Reviews Case Reports Research Article

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Articles

Amniocentesis in the West Midlands: report on 1000 births
Tessa Webb, J H Edwards, A H Cameron, J Margaret Crawley, Maj Hulten, D I Rushton, and R A Thompson
J Med Genet 1980; 17: 81-86. doi:10.1136/jmg.17.2.81 [Abstract] [PDF] [Request Permissions]

Papers presented at the Clinical Genetics Society meeting, 15—16 November 1979
J Med Genet 1980; 17: 156. doi:10.1136/jmg.17.2.156 [PDF] [Request Permissions]

Correspondence

HLA Bw35 antigen and human reproduction
Maria Purpura, Isa Coghi, Maria Nicotra, Erminia Carapella, and E. Bottini
J Med Genet 1980; 17: 157. doi:10.1136/jmg.17.2.157 [PDF] [Request Permissions]

John Fraser Roberts's 80th birthday
Paul E Polani and Colleagues
J Med Genet 1980; 17: 158. doi:10.1136/jmg.17.2.158-a [PDF] [Request Permissions]

Book Reviews

Mutagenesis in Sub-Mammalian Systems: Status and Significance
D G Harnden
J Med Genet 1980; 17: 159. doi:10.1136/jmg.17.2.159 [PDF] [Request Permissions]

Genetic Mosaics and Chimeras in Mammals
Christine Gosden
J Med Genet 1980; 17: 159-160. doi:10.1136/jmg.17.2.159-a [PDF] [Request Permissions]

The Neutrophil: Function and Clinical Disorders
Roland Levinsky
J Med Genet 1980; 17: 160. doi:10.1136/jmg.17.2.160 [PDF] [Request Permissions]

Case Reports

Ring chromosome 10: 46,XX,r(10)(p15 $->$ q26)
Ryuichi Tsukino, Norihiko Tsuda, Tohru Dezawa, Tadashi Ishii, and Michio Koike
J Med Genet 1980; 17: 148-151. doi:10.1136/jmg.17.2.148 [Abstract] [PDF] [Request Permissions]

A case of Klinefelter's syndrome with 47,Xi(Xq)Y karyotype
G Ponzio, M DeMarchi, G Gallone, D Fonzo, and A O Carbonara
J Med Genet 1980; 17: 152-155. doi:10.1136/jmg.17.2.152 [Abstract] [PDF] [Request Permissions]

Research Article

Risk of recurrence after two children with central nervous system malformations in an area of high incidence.
N C Nevin and W P Johnston
J Med Genet 1980; 17: 87-92. doi:10.1136/jmg.17.2.87 [Abstract] [PDF] [Request Permissions]

Concordance rates in twins for anencephaly.
W H James
J Med Genet 1980; 17: 93-94. doi:10.1136/jmg.17.2.93 [Abstract] [PDF] [Request Permissions]

Excess of cancer deaths in grandparents of patients with retinoblastoma.
C Bonaïti-Pellié and M L Briard-Guillemot
J Med Genet 1980; 17: 95-101. doi:10.1136/jmg.17.2.95 [Abstract] [PDF] [Request Permissions]

A family and population study of the genetic polymorphism of debrisoquine oxidation in a white British population.
D A Evans, A Mahgoub, T P Sloan, J R Idle, and R L Smith
J Med Genet 1980; 17: 102-105. doi:10.1136/jmg.17.2.102 [Abstract] [PDF] [Request Permissions]

No sex difference in mutations rates of Duchenne muscular dystrophy.
N Yasuda and K Kondô
J Med Genet 1980; 17: 106-111. doi:10.1136/jmg.17.2.106 [Abstract] [PDF] [Request Permissions]

Parental factors associated with rigidity in Huntington's disease.
C J Brackenridge
J Med Genet 1980; 17: 112-114. doi:10.1136/jmg.17.2.112 [Abstract] [PDF] [Request Permissions]

Familial cerebellar ataxia presenting with down beat nystagmus.
G D Schott
J Med Genet 1980; 17: 115-118. doi:10.1136/jmg.17.2.115 [Abstract] [PDF] [Request Permissions]

Syndrome of polydactyly, cleft lip/palate or lingual lump, and psychomotor retardation in endogamic gypsies.
V Váradi, L Szabó, and Z Papp
J Med Genet 1980; 17: 119-122. doi:10.1136/jmg.17.2.119 [Abstract] [PDF] [Request Permissions]

Recessive aplasia cutis congenita of the limbs.
N Freire-Maia, M Pinheiro, and C C Ortega
J Med Genet 1980; 17: 123-126. doi:10.1136/jmg.17.2.123 [Abstract] [PDF] [Request Permissions]

An epidemiological study of facial clefting in Manitoba.
J Welch and A G Hunter
J Med Genet 1980; 17: 127-132. doi:10.1136/jmg.17.2.127 [Abstract] [PDF] [Request Permissions]

Partial anomalous pulmonary venous drainage in two patients with Turner's syndrome.
W H Price and R F Willey
J Med Genet 1980; 17: 133-134. doi:10.1136/jmg.17.2.133 [Abstract] [PDF] [Request Permissions]

Diaphragmatic hernia in Avon.
T J David, V M Parker, and C A Illingworth
J Med Genet 1980; 17: 135. doi:10.1136/jmg.17.2.135 [Abstract] [PDF] [Request Permissions]

Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling.
A C Berry, E M Belton, and C Chantler
J Med Genet 1980; 17: 136-138. doi:10.1136/jmg.17.2.136 [Abstract] [PDF] [Request Permissions]

A family study of bladder exstrophy.
E Ives, R Coffey, and C O Carter
J Med Genet 1980; 17: 139-141. doi:10.1136/jmg.17.2.139 [Abstract] [PDF] [Request Permissions]

Dermatoglyphs and chromosome mosaicism in parents of children with trisomy 18.
M Holmes-Siedle, S Kerr, R H Lindenbaum, and M Bobrow
J Med Genet 1980; 17: 142-143. doi:10.1136/jmg.17.2.142 [Abstract] [PDF] [Request Permissions]

Dic(21;21) in a Down's syndrome child with an unusual chromosome 9 variant in the mother.
J M Berg, H A Gardner, R J Gardner, E G Goh, V D Markovic, N E Simpson, and R G Worton
J Med Genet 1980; 17: 144-148. doi:10.1136/jmg.17.2.144 [Abstract] [PDF] [Request Permissions]

Hypomelanosis of Ito with triphalangeal thumbs.
M K Kukolich, B W Althaus, M V Freeman, and R C Lewandowski
J Med Genet 1980; 17: 151-152. doi:10.1136/jmg.17.2.151 [Abstract] [PDF] [Request Permissions]

HLA Bw35 antigen and human reproduction.
M Purpura, I Coghi, M Nicotra, E Carapella, and E Bottini
J Med Genet 1980; 17: 157-158. doi:10.1136/jmg.17.2.157-a [PDF] [Request Permissions]

Prenatal study of X-linked aqueductal stenosis.
P Benke and R Strassberg
J Med Genet 1980; 17: 158. doi:10.1136/jmg.17.2.158 [PDF] [Request Permissions]

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	Amniocentesis in the West Midlands: report on 1000 births Tessa Webb, J H Edwards, A H Cameron, J Margaret Crawley, Maj Hulten, D I Rushton, and R A Thompson J Med Genet 1980; 17: 81-86. doi:10.1136/jmg.17.2.81 [Abstract] [PDF] [Request Permissions]

	Papers presented at the Clinical Genetics Society meeting, 15—16 November 1979 J Med Genet 1980; 17: 156. doi:10.1136/jmg.17.2.156 [PDF] [Request Permissions]

	HLA Bw35 antigen and human reproduction Maria Purpura, Isa Coghi, Maria Nicotra, Erminia Carapella, and E. Bottini J Med Genet 1980; 17: 157. doi:10.1136/jmg.17.2.157 [PDF] [Request Permissions]

	John Fraser Roberts's 80th birthday Paul E Polani and Colleagues J Med Genet 1980; 17: 158. doi:10.1136/jmg.17.2.158-a [PDF] [Request Permissions]

	Mutagenesis in Sub-Mammalian Systems: Status and Significance D G Harnden J Med Genet 1980; 17: 159. doi:10.1136/jmg.17.2.159 [PDF] [Request Permissions]

	Genetic Mosaics and Chimeras in Mammals Christine Gosden J Med Genet 1980; 17: 159-160. doi:10.1136/jmg.17.2.159-a [PDF] [Request Permissions]

	The Neutrophil: Function and Clinical Disorders Roland Levinsky J Med Genet 1980; 17: 160. doi:10.1136/jmg.17.2.160 [PDF] [Request Permissions]

	Ring chromosome 10: 46,XX,r(10)(p15 $->$ q26) Ryuichi Tsukino, Norihiko Tsuda, Tohru Dezawa, Tadashi Ishii, and Michio Koike J Med Genet 1980; 17: 148-151. doi:10.1136/jmg.17.2.148 [Abstract] [PDF] [Request Permissions]

	A case of Klinefelter's syndrome with 47,Xi(Xq)Y karyotype G Ponzio, M DeMarchi, G Gallone, D Fonzo, and A O Carbonara J Med Genet 1980; 17: 152-155. doi:10.1136/jmg.17.2.152 [Abstract] [PDF] [Request Permissions]

	Risk of recurrence after two children with central nervous system malformations in an area of high incidence. N C Nevin and W P Johnston J Med Genet 1980; 17: 87-92. doi:10.1136/jmg.17.2.87 [Abstract] [PDF] [Request Permissions]

	Concordance rates in twins for anencephaly. W H James J Med Genet 1980; 17: 93-94. doi:10.1136/jmg.17.2.93 [Abstract] [PDF] [Request Permissions]

	Excess of cancer deaths in grandparents of patients with retinoblastoma. C Bonaïti-Pellié and M L Briard-Guillemot J Med Genet 1980; 17: 95-101. doi:10.1136/jmg.17.2.95 [Abstract] [PDF] [Request Permissions]

	A family and population study of the genetic polymorphism of debrisoquine oxidation in a white British population. D A Evans, A Mahgoub, T P Sloan, J R Idle, and R L Smith J Med Genet 1980; 17: 102-105. doi:10.1136/jmg.17.2.102 [Abstract] [PDF] [Request Permissions]

	No sex difference in mutations rates of Duchenne muscular dystrophy. N Yasuda and K Kondô J Med Genet 1980; 17: 106-111. doi:10.1136/jmg.17.2.106 [Abstract] [PDF] [Request Permissions]

	Parental factors associated with rigidity in Huntington's disease. C J Brackenridge J Med Genet 1980; 17: 112-114. doi:10.1136/jmg.17.2.112 [Abstract] [PDF] [Request Permissions]

	Familial cerebellar ataxia presenting with down beat nystagmus. G D Schott J Med Genet 1980; 17: 115-118. doi:10.1136/jmg.17.2.115 [Abstract] [PDF] [Request Permissions]

	Syndrome of polydactyly, cleft lip/palate or lingual lump, and psychomotor retardation in endogamic gypsies. V Váradi, L Szabó, and Z Papp J Med Genet 1980; 17: 119-122. doi:10.1136/jmg.17.2.119 [Abstract] [PDF] [Request Permissions]

	Recessive aplasia cutis congenita of the limbs. N Freire-Maia, M Pinheiro, and C C Ortega J Med Genet 1980; 17: 123-126. doi:10.1136/jmg.17.2.123 [Abstract] [PDF] [Request Permissions]

	An epidemiological study of facial clefting in Manitoba. J Welch and A G Hunter J Med Genet 1980; 17: 127-132. doi:10.1136/jmg.17.2.127 [Abstract] [PDF] [Request Permissions]

	Partial anomalous pulmonary venous drainage in two patients with Turner's syndrome. W H Price and R F Willey J Med Genet 1980; 17: 133-134. doi:10.1136/jmg.17.2.133 [Abstract] [PDF] [Request Permissions]

	Diaphragmatic hernia in Avon. T J David, V M Parker, and C A Illingworth J Med Genet 1980; 17: 135. doi:10.1136/jmg.17.2.135 [Abstract] [PDF] [Request Permissions]

	Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling. A C Berry, E M Belton, and C Chantler J Med Genet 1980; 17: 136-138. doi:10.1136/jmg.17.2.136 [Abstract] [PDF] [Request Permissions]

	A family study of bladder exstrophy. E Ives, R Coffey, and C O Carter J Med Genet 1980; 17: 139-141. doi:10.1136/jmg.17.2.139 [Abstract] [PDF] [Request Permissions]

	Dermatoglyphs and chromosome mosaicism in parents of children with trisomy 18. M Holmes-Siedle, S Kerr, R H Lindenbaum, and M Bobrow J Med Genet 1980; 17: 142-143. doi:10.1136/jmg.17.2.142 [Abstract] [PDF] [Request Permissions]

	Dic(21;21) in a Down's syndrome child with an unusual chromosome 9 variant in the mother. J M Berg, H A Gardner, R J Gardner, E G Goh, V D Markovic, N E Simpson, and R G Worton J Med Genet 1980; 17: 144-148. doi:10.1136/jmg.17.2.144 [Abstract] [PDF] [Request Permissions]

	Hypomelanosis of Ito with triphalangeal thumbs. M K Kukolich, B W Althaus, M V Freeman, and R C Lewandowski J Med Genet 1980; 17: 151-152. doi:10.1136/jmg.17.2.151 [Abstract] [PDF] [Request Permissions]

	HLA Bw35 antigen and human reproduction. M Purpura, I Coghi, M Nicotra, E Carapella, and E Bottini J Med Genet 1980; 17: 157-158. doi:10.1136/jmg.17.2.157-a [PDF] [Request Permissions]

	Prenatal study of X-linked aqueductal stenosis. P Benke and R Strassberg J Med Genet 1980; 17: 158. doi:10.1136/jmg.17.2.158 [PDF] [Request Permissions]