J Med Genet -- Table of Contents (16 [1])

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February 1979 (Volume 16, Number 1). [Index by author]

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Articles

Inbreeding effects on fertility and sterility in southern India
P. S. S. Rao and S. G. Inbaraj
J Med Genet 1979; 16: 24-31. doi:10.1136/jmg.16.1.24 [Abstract] [PDF] [Request Permissions]

Classification and identification of inherited brachydactylies
Naomi Fitch
J Med Genet 1979; 16: 36-44. doi:10.1136/jmg.16.1.36 [Abstract] [PDF] [Request Permissions]

Recessive anonychia totalis and dominant aplasia (or hypoplasia) of upper lateral incisors in the same kindred
N. Freire-Maia and Marta Pinheiro
J Med Genet 1979; 16: 45-48. doi:10.1136/jmg.16.1.45 [Abstract] [PDF] [Request Permissions]

Book Reviews

Foetus into Man. Physical Growth from Conception to Maturity
C. O. Carter
J Med Genet 1979; 16: 81. doi:10.1136/jmg.16.1.81 [PDF] [Request Permissions]

Introduction to Biological Scanning Electron Microscopy
Patricia R. Mann
J Med Genet 1979; 16: 81-82. doi:10.1136/jmg.16.1.81-a [PDF] [Request Permissions]

The Hemoglobinopathies. Techniques of Identification: Clinical and Biochemical Analysis, Vol. 6
Marcus Pembrey
J Med Genet 1979; 16: 82-83. doi:10.1136/jmg.16.1.82 [PDF] [Request Permissions]

Dermatoglyphics. An International Bibliography
T. J. David
J Med Genet 1979; 16: 83. doi:10.1136/jmg.16.1.83 [PDF] [Request Permissions]

The Genetic Approach to Human Disease
C. O. Carter
J Med Genet 1979; 16: 83. doi:10.1136/jmg.16.1.83-a [PDF] [Request Permissions]

Research Article

Familial polyposis coli: heterogeneous polyp expression in 2 kindreds.
H T Lynch, P M Lynch, K L Follett, and R E Harris
J Med Genet 1979; 16: 1-7. doi:10.1136/jmg.16.1.1 [Abstract] [PDF] [Request Permissions]

Neural tube malformations: complex segregation analysis and calculation of recurrence risks.
J M Lalouel, N E Morton, and J Jackson
J Med Genet 1979; 16: 8-13. doi:10.1136/jmg.16.1.8 [Abstract] [PDF] [Request Permissions]

Sib risk of neural tube defect: is prenatal diagnosis indicated in pregnancies following the birth of a hydrocephalic child?
T Cohen, E Stern, and A Rosenmann
J Med Genet 1979; 16: 14-16. doi:10.1136/jmg.16.1.14 [Abstract] [PDF] [Request Permissions]

Familial caudal regression anomalad and maternal diabetes.
J M Stewart and S Stoll
J Med Genet 1979; 16: 17-20. doi:10.1136/jmg.16.1.17 [Abstract] [PDF] [Request Permissions]

Tissue typing amniotic fluid cells: potential use for detection of contaminating maternal cells.
M Niazi, D V Coleman, J F Mowbray, and S Blunt
J Med Genet 1979; 16: 21-23. doi:10.1136/jmg.16.1.21 [Abstract] [PDF] [Request Permissions]

Tuberous sclerosis: possible modification of phenotypic expression by an unlinked dominant gene.
A R Rushton and B A Shaywitz
J Med Genet 1979; 16: 32-35. doi:10.1136/jmg.16.1.32 [Abstract] [PDF] [Request Permissions]

Serum creatine kinase levels in normal females.
R K Satapathy and R Skinner
J Med Genet 1979; 16: 49-51. doi:10.1136/jmg.16.1.49 [Abstract] [PDF] [Request Permissions]

Beta-thalassaemia: increased chromosomal anomalies in lymphocyte cultures.
G B Côté and S Papadakou-Lagoyanni
J Med Genet 1979; 16: 52-55. doi:10.1136/jmg.16.1.52 [Abstract] [PDF] [Request Permissions]

Meiosis in two human reciprocal translocations.
C S Román,, M T Sordo, and J M García-Sagredo
J Med Genet 1979; 16: 56-59. doi:10.1136/jmg.16.1.56 [Abstract] [PDF] [Request Permissions]

Familial partial 14 trisomy.
J Q Miller, K Willson, H Wyandt, M A Jaramillo, and T S McConnell
J Med Genet 1979; 16: 60-65. doi:10.1136/jmg.16.1.60 [Abstract] [PDF] [Request Permissions]

Abnormal children of a 47,XYY father.
C Stoll, E Flori, A Clavert, D Beshara, and P Buck
J Med Genet 1979; 16: 66-68. doi:10.1136/jmg.16.1.66 [Abstract] [PDF] [Request Permissions]

Extra small metacentric chromosome identified as i(18p).
M Rocchi, M Stormi, N Archidiacono, and G Filippi
J Med Genet 1979; 16: 69-73. doi:10.1136/jmg.16.1.69 [Abstract] [PDF] [Request Permissions]

Familial dicentric translocation t(13;18)(p13;p11.2) ascertained by recurrent miscarriages.
A Daniel, I D Perel, A J Clarke, and T Saville
J Med Genet 1979; 16: 73-75. doi:10.1136/jmg.16.1.73 [Abstract] [PDF] [Request Permissions]

The 9p-syndrome.
S J Funderburk, R S Sparkes, and I Klisak
J Med Genet 1979; 16: 75-79. doi:10.1136/jmg.16.1.75 [Abstract] [PDF] [Request Permissions]

Variation in chromosome 19.
H A Gardner and E M Wood
J Med Genet 1979; 16: 79-80. doi:10.1136/jmg.16.1.79 [Abstract] [PDF] [Request Permissions]

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	Inbreeding effects on fertility and sterility in southern India P. S. S. Rao and S. G. Inbaraj J Med Genet 1979; 16: 24-31. doi:10.1136/jmg.16.1.24 [Abstract] [PDF] [Request Permissions]

	Classification and identification of inherited brachydactylies Naomi Fitch J Med Genet 1979; 16: 36-44. doi:10.1136/jmg.16.1.36 [Abstract] [PDF] [Request Permissions]

	Recessive anonychia totalis and dominant aplasia (or hypoplasia) of upper lateral incisors in the same kindred N. Freire-Maia and Marta Pinheiro J Med Genet 1979; 16: 45-48. doi:10.1136/jmg.16.1.45 [Abstract] [PDF] [Request Permissions]

	Foetus into Man. Physical Growth from Conception to Maturity C. O. Carter J Med Genet 1979; 16: 81. doi:10.1136/jmg.16.1.81 [PDF] [Request Permissions]

	Introduction to Biological Scanning Electron Microscopy Patricia R. Mann J Med Genet 1979; 16: 81-82. doi:10.1136/jmg.16.1.81-a [PDF] [Request Permissions]

	The Hemoglobinopathies. Techniques of Identification: Clinical and Biochemical Analysis, Vol. 6 Marcus Pembrey J Med Genet 1979; 16: 82-83. doi:10.1136/jmg.16.1.82 [PDF] [Request Permissions]

	Dermatoglyphics. An International Bibliography T. J. David J Med Genet 1979; 16: 83. doi:10.1136/jmg.16.1.83 [PDF] [Request Permissions]

	The Genetic Approach to Human Disease C. O. Carter J Med Genet 1979; 16: 83. doi:10.1136/jmg.16.1.83-a [PDF] [Request Permissions]

	Familial polyposis coli: heterogeneous polyp expression in 2 kindreds. H T Lynch, P M Lynch, K L Follett, and R E Harris J Med Genet 1979; 16: 1-7. doi:10.1136/jmg.16.1.1 [Abstract] [PDF] [Request Permissions]

	Neural tube malformations: complex segregation analysis and calculation of recurrence risks. J M Lalouel, N E Morton, and J Jackson J Med Genet 1979; 16: 8-13. doi:10.1136/jmg.16.1.8 [Abstract] [PDF] [Request Permissions]

	Sib risk of neural tube defect: is prenatal diagnosis indicated in pregnancies following the birth of a hydrocephalic child? T Cohen, E Stern, and A Rosenmann J Med Genet 1979; 16: 14-16. doi:10.1136/jmg.16.1.14 [Abstract] [PDF] [Request Permissions]

	Familial caudal regression anomalad and maternal diabetes. J M Stewart and S Stoll J Med Genet 1979; 16: 17-20. doi:10.1136/jmg.16.1.17 [Abstract] [PDF] [Request Permissions]

	Tissue typing amniotic fluid cells: potential use for detection of contaminating maternal cells. M Niazi, D V Coleman, J F Mowbray, and S Blunt J Med Genet 1979; 16: 21-23. doi:10.1136/jmg.16.1.21 [Abstract] [PDF] [Request Permissions]

	Tuberous sclerosis: possible modification of phenotypic expression by an unlinked dominant gene. A R Rushton and B A Shaywitz J Med Genet 1979; 16: 32-35. doi:10.1136/jmg.16.1.32 [Abstract] [PDF] [Request Permissions]

	Serum creatine kinase levels in normal females. R K Satapathy and R Skinner J Med Genet 1979; 16: 49-51. doi:10.1136/jmg.16.1.49 [Abstract] [PDF] [Request Permissions]

	Beta-thalassaemia: increased chromosomal anomalies in lymphocyte cultures. G B Côté and S Papadakou-Lagoyanni J Med Genet 1979; 16: 52-55. doi:10.1136/jmg.16.1.52 [Abstract] [PDF] [Request Permissions]

	Meiosis in two human reciprocal translocations. C S Román,, M T Sordo, and J M García-Sagredo J Med Genet 1979; 16: 56-59. doi:10.1136/jmg.16.1.56 [Abstract] [PDF] [Request Permissions]

	Familial partial 14 trisomy. J Q Miller, K Willson, H Wyandt, M A Jaramillo, and T S McConnell J Med Genet 1979; 16: 60-65. doi:10.1136/jmg.16.1.60 [Abstract] [PDF] [Request Permissions]

	Abnormal children of a 47,XYY father. C Stoll, E Flori, A Clavert, D Beshara, and P Buck J Med Genet 1979; 16: 66-68. doi:10.1136/jmg.16.1.66 [Abstract] [PDF] [Request Permissions]

	Extra small metacentric chromosome identified as i(18p). M Rocchi, M Stormi, N Archidiacono, and G Filippi J Med Genet 1979; 16: 69-73. doi:10.1136/jmg.16.1.69 [Abstract] [PDF] [Request Permissions]

	Familial dicentric translocation t(13;18)(p13;p11.2) ascertained by recurrent miscarriages. A Daniel, I D Perel, A J Clarke, and T Saville J Med Genet 1979; 16: 73-75. doi:10.1136/jmg.16.1.73 [Abstract] [PDF] [Request Permissions]

	The 9p-syndrome. S J Funderburk, R S Sparkes, and I Klisak J Med Genet 1979; 16: 75-79. doi:10.1136/jmg.16.1.75 [Abstract] [PDF] [Request Permissions]

	Variation in chromosome 19. H A Gardner and E M Wood J Med Genet 1979; 16: 79-80. doi:10.1136/jmg.16.1.79 [Abstract] [PDF] [Request Permissions]