J Med Genet -- Table of Contents (15 [1])

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February 1978 (Volume 15, Number 1). [Index by author]

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Articles

Genetic family history questionnaire
June Cole, P. Michael Conneally, M. E. Hodes, and A. D. Merritt
J Med Genet 1978; 15: 10-18. doi:10.1136/jmg.15.1.10 [Abstract] [PDF] [Request Permissions]

Book Reviews

Down's Anomaly 2nd ed
M. Baraitser
J Med Genet 1978; 15: 79. doi:10.1136/jmg.15.1.79 [PDF] [Request Permissions]

Principles of Genetic Counselling
Cedric Carter
J Med Genet 1978; 15: 79-80. doi:10.1136/jmg.15.1.79-a [PDF] [Request Permissions]

Experimental Biology and Medicine Cytogenetic aspects of Malignant Transformation
B. R. Reeves
J Med Genet 1978; 15: 80. doi:10.1136/jmg.15.1.80 [PDF] [Request Permissions]

Chemical Mutagens. Principles and Methods for their Detection Vol. 4
B. A. Bridges
J Med Genet 1978; 15: 80-81. doi:10.1136/jmg.15.1.80-a [PDF] [Request Permissions]

Population Cytogenetics: Studies in Humans
C. E. Blank
J Med Genet 1978; 15: 81-82. doi:10.1136/jmg.15.1.81 [PDF] [Request Permissions]

Dermatoglyphics in Medical Disorders
B. W. Richards
J Med Genet 1978; 15: 82-83. doi:10.1136/jmg.15.1.82 [PDF] [Request Permissions]

Medico-Social Management of Inherited Metabolic Disease
Rodney Harris
J Med Genet 1978; 15: 83. doi:10.1136/jmg.15.1.83 [PDF] [Request Permissions]

Atlas des Maladies Chromosomiques
M. Baraitser
J Med Genet 1978; 15: 84. doi:10.1136/jmg.15.1.84 [PDF] [Request Permissions]

Advances in Human Genetics. Vol. 7
Peter S. Harper
J Med Genet 1978; 15: 84. doi:10.1136/jmg.15.1.84-a [PDF] [Request Permissions]

Research Article

Simplified classification of spontaneous abortions.
D I Rushton
J Med Genet 1978; 15: 1-9. doi:10.1136/jmg.15.1.1 [Abstract] [PDF] [Request Permissions]

Comment.
R Harris
J Med Genet 1978; 15: 19. doi:10.1136/jmg.15.1.19 [PDF] [Request Permissions]

Risk of coeliac disease in children of patients and effect of HLA genotype.
N R Dennis and C R Stokes
J Med Genet 1978; 15: 20-22. doi:10.1136/jmg.15.1.20 [Abstract] [PDF] [Request Permissions]

Validation and aplication of an interval factor in estimating age at onset of Huntington's disease.
C J Brackenridge
J Med Genet 1978; 15: 23-26. doi:10.1136/jmg.15.1.23 [Abstract] [PDF] [Request Permissions]

E1k, another quantitative variant at cholinesterase locus 1.
H M Rubinstein, A A Dietz, and T Lubrano
J Med Genet 1978; 15: 27-29. doi:10.1136/jmg.15.1.27 [Abstract] [PDF] [Request Permissions]

The Axenfeld syndrome and the Rieger syndrome.
N Fitch and M Kaback
J Med Genet 1978; 15: 30-34. doi:10.1136/jmg.15.1.30 [Abstract] [PDF] [Request Permissions]

Popliteal pterygium syndrome: a phenotypic and genetic analysis.
V Escobar and D Weaver
J Med Genet 1978; 15: 35-42. doi:10.1136/jmg.15.1.35 [Abstract] [PDF] [Request Permissions]

Down syndrome and recent demographic trends in Manitoba.
J A Evans, A G Hunter, and J L Hamerton
J Med Genet 1978; 15: 43-47. doi:10.1136/jmg.15.1.43 [Abstract] [PDF] [Request Permissions]

Clinical experience with trisomies 18 and 13.
M E Hodes, J Cole, C G Palmer, and T Reed
J Med Genet 1978; 15: 48-60. doi:10.1136/jmg.15.1.48 [Abstract] [PDF] [Request Permissions]

Raised alpha-fetoprotein levels in amniotic fluid and maternal serum associated with distension of the fetal bladder caused by absence of urethra.
N C Nevin, A Ritchie, F McKeown, and G Roberts
J Med Genet 1978; 15: 61-63. doi:10.1136/jmg.15.1.61 [Abstract] [PDF] [Request Permissions]

Primary hypogonadism in the Borjeson-Forssman-Lehmann syndrome.
F T Weber, J L Frias, R L Julius, and A H Felman
J Med Genet 1978; 15: 63-66. doi:10.1136/jmg.15.1.63 [Abstract] [PDF] [Request Permissions]

Waardenburg-like features with cataracts, small head size, joint abnormalities, hypogonadism, and osteosarcoma.
D M Parry, A W Safyer, and J J Mulvihill
J Med Genet 1978; 15: 66-69. doi:10.1136/jmg.15.1.66 [Abstract] [PDF] [Request Permissions]

Trisomy 8 syndrome.
A R Gagliardi, E H Tajara, M Varella-Garcia, and L M Moreira
J Med Genet 1978; 15: 70-73. doi:10.1136/jmg.15.1.70 [Abstract] [PDF] [Request Permissions]

Trisomy 18 syndrome with an unusual karyotype: possible double isochromosome.
L M Larson, W A Wasdahl, J H Saumur, M L Coleman, and S M Jalal
J Med Genet 1978; 15: 73-76. doi:10.1136/jmg.15.1.73 [Abstract] [PDF] [Request Permissions]

Partial 18 trisomy (with 47 chromosomes) resulting from a familial maternal translocation.
K Fried, A Bar-Yochai, M Rosenblatt, and G Mundel
J Med Genet 1978; 15: 76-78. doi:10.1136/jmg.15.1.76 [Abstract] [PDF] [Request Permissions]

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	Genetic family history questionnaire June Cole, P. Michael Conneally, M. E. Hodes, and A. D. Merritt J Med Genet 1978; 15: 10-18. doi:10.1136/jmg.15.1.10 [Abstract] [PDF] [Request Permissions]

	Down's Anomaly 2nd ed M. Baraitser J Med Genet 1978; 15: 79. doi:10.1136/jmg.15.1.79 [PDF] [Request Permissions]

	Principles of Genetic Counselling Cedric Carter J Med Genet 1978; 15: 79-80. doi:10.1136/jmg.15.1.79-a [PDF] [Request Permissions]

	Experimental Biology and Medicine Cytogenetic aspects of Malignant Transformation B. R. Reeves J Med Genet 1978; 15: 80. doi:10.1136/jmg.15.1.80 [PDF] [Request Permissions]

	Chemical Mutagens. Principles and Methods for their Detection Vol. 4 B. A. Bridges J Med Genet 1978; 15: 80-81. doi:10.1136/jmg.15.1.80-a [PDF] [Request Permissions]

	Population Cytogenetics: Studies in Humans C. E. Blank J Med Genet 1978; 15: 81-82. doi:10.1136/jmg.15.1.81 [PDF] [Request Permissions]

	Dermatoglyphics in Medical Disorders B. W. Richards J Med Genet 1978; 15: 82-83. doi:10.1136/jmg.15.1.82 [PDF] [Request Permissions]

	Medico-Social Management of Inherited Metabolic Disease Rodney Harris J Med Genet 1978; 15: 83. doi:10.1136/jmg.15.1.83 [PDF] [Request Permissions]

	Atlas des Maladies Chromosomiques M. Baraitser J Med Genet 1978; 15: 84. doi:10.1136/jmg.15.1.84 [PDF] [Request Permissions]

	Advances in Human Genetics. Vol. 7 Peter S. Harper J Med Genet 1978; 15: 84. doi:10.1136/jmg.15.1.84-a [PDF] [Request Permissions]

	Simplified classification of spontaneous abortions. D I Rushton J Med Genet 1978; 15: 1-9. doi:10.1136/jmg.15.1.1 [Abstract] [PDF] [Request Permissions]

	Comment. R Harris J Med Genet 1978; 15: 19. doi:10.1136/jmg.15.1.19 [PDF] [Request Permissions]

	Risk of coeliac disease in children of patients and effect of HLA genotype. N R Dennis and C R Stokes J Med Genet 1978; 15: 20-22. doi:10.1136/jmg.15.1.20 [Abstract] [PDF] [Request Permissions]

	Validation and aplication of an interval factor in estimating age at onset of Huntington's disease. C J Brackenridge J Med Genet 1978; 15: 23-26. doi:10.1136/jmg.15.1.23 [Abstract] [PDF] [Request Permissions]

	E1k, another quantitative variant at cholinesterase locus 1. H M Rubinstein, A A Dietz, and T Lubrano J Med Genet 1978; 15: 27-29. doi:10.1136/jmg.15.1.27 [Abstract] [PDF] [Request Permissions]

	The Axenfeld syndrome and the Rieger syndrome. N Fitch and M Kaback J Med Genet 1978; 15: 30-34. doi:10.1136/jmg.15.1.30 [Abstract] [PDF] [Request Permissions]

	Popliteal pterygium syndrome: a phenotypic and genetic analysis. V Escobar and D Weaver J Med Genet 1978; 15: 35-42. doi:10.1136/jmg.15.1.35 [Abstract] [PDF] [Request Permissions]

	Down syndrome and recent demographic trends in Manitoba. J A Evans, A G Hunter, and J L Hamerton J Med Genet 1978; 15: 43-47. doi:10.1136/jmg.15.1.43 [Abstract] [PDF] [Request Permissions]

	Clinical experience with trisomies 18 and 13. M E Hodes, J Cole, C G Palmer, and T Reed J Med Genet 1978; 15: 48-60. doi:10.1136/jmg.15.1.48 [Abstract] [PDF] [Request Permissions]

	Raised alpha-fetoprotein levels in amniotic fluid and maternal serum associated with distension of the fetal bladder caused by absence of urethra. N C Nevin, A Ritchie, F McKeown, and G Roberts J Med Genet 1978; 15: 61-63. doi:10.1136/jmg.15.1.61 [Abstract] [PDF] [Request Permissions]

	Primary hypogonadism in the Borjeson-Forssman-Lehmann syndrome. F T Weber, J L Frias, R L Julius, and A H Felman J Med Genet 1978; 15: 63-66. doi:10.1136/jmg.15.1.63 [Abstract] [PDF] [Request Permissions]

	Waardenburg-like features with cataracts, small head size, joint abnormalities, hypogonadism, and osteosarcoma. D M Parry, A W Safyer, and J J Mulvihill J Med Genet 1978; 15: 66-69. doi:10.1136/jmg.15.1.66 [Abstract] [PDF] [Request Permissions]

	Trisomy 8 syndrome. A R Gagliardi, E H Tajara, M Varella-Garcia, and L M Moreira J Med Genet 1978; 15: 70-73. doi:10.1136/jmg.15.1.70 [Abstract] [PDF] [Request Permissions]

	Trisomy 18 syndrome with an unusual karyotype: possible double isochromosome. L M Larson, W A Wasdahl, J H Saumur, M L Coleman, and S M Jalal J Med Genet 1978; 15: 73-76. doi:10.1136/jmg.15.1.73 [Abstract] [PDF] [Request Permissions]

	Partial 18 trisomy (with 47 chromosomes) resulting from a familial maternal translocation. K Fried, A Bar-Yochai, M Rosenblatt, and G Mundel J Med Genet 1978; 15: 76-78. doi:10.1136/jmg.15.1.76 [Abstract] [PDF] [Request Permissions]