J Med Genet -- Table of Contents (15 [2])

Subscribe here
Activate your subscription

Home > Volume 15, Number 2

Only Abstracts and PDFs available for this issue

Other Issues:
April 1978 (Volume 15, Number 2). [Index by author]

		Articles Articles Research Article

Find articles in this issue containing these words: [Search ALL Issues]

Table of Contents (PDF) | Cover (PDF) | Administration (PDF)

To see an article, click its [Full Text] link. To review many abstracts, check the boxes to the left of the titles you want, and click the 'Get All Checked Abstracts' button. To see one abstract at a time, click its [Abstract] link.

Articles

A family study of vesicoureteric reflux
Aida De Vargas, Kathleen Evans, P. Ransley, A. R. Rosenberg, D. Rothwell, T. Sherwood, D. I. Williams, T. M. Barratt, and C. O. Carter
J Med Genet 1978; 15: 85-96. doi:10.1136/jmg.15.2.85 [Abstract] [PDF] [Request Permissions]

Research Article

Cellular content of amniotic fluid as predictor of central nervous system malformations.
M Bobrow, C J Evans, J Noble, and C Patel
J Med Genet 1978; 15: 97-100. doi:10.1136/jmg.15.2.97 [Abstract] [PDF] [Request Permissions]

Shifting genetic patterns in anencephaly and spina bifida.
D T Janerich and J Piper
J Med Genet 1978; 15: 101-105. doi:10.1136/jmg.15.2.101 [Abstract] [PDF] [Request Permissions]

Use of overlapping normal distributions in genetic counselling.
N R Dennis and C O Carter
J Med Genet 1978; 15: 106-108. doi:10.1136/jmg.15.2.106 [Abstract] [PDF] [Request Permissions]

Genetic counseling of consanguineous families. Use of Smith's method to calculate recurrence risks in multifactorial inheritance in consanguineous matings.
C Bonaiti
J Med Genet 1978; 15: 109-112. doi:10.1136/jmg.15.2.109 [Abstract] [PDF] [Request Permissions]

Linkage relations of a locus for congenital total nuclear cataract.
R S Huntzinger, L R Weitkamp, and P D Roca
J Med Genet 1978; 15: 113-115. doi:10.1136/jmg.15.2.113 [Abstract] [PDF] [Request Permissions]

Unusual inheritance of Becker type muscular dystrophy.
L Aguilar, R Lisker, and G G Ramos
J Med Genet 1978; 15: 116-118. doi:10.1136/jmg.15.2.116 [Abstract] [PDF] [Request Permissions]

Hereditary brachydactyly with nail dysplasia.
G D Schott
J Med Genet 1978; 15: 119-122. doi:10.1136/jmg.15.2.119 [Abstract] [PDF] [Request Permissions]

Recessively inherited costovertebral segmentation defect with mesomelia and peculiar facies (Covesdem syndrome): A new genetic entity?
R S Wadia, D B Shirole, and M S Dikshit
J Med Genet 1978; 15: 123-127. doi:10.1136/jmg.15.2.123 [Abstract] [PDF] [Request Permissions]

A new type of chondrodystrophic mutant in the mouse.
J M Ferguson, M E Wallace, and D R Johnson
J Med Genet 1978; 15: 128-131. doi:10.1136/jmg.15.2.128 [Abstract] [PDF] [Request Permissions]

Fertility in 47,XXX and 45,X patients.
J Dewhurst
J Med Genet 1978; 15: 132-135. doi:10.1136/jmg.15.2.132 [Abstract] [PDF] [Request Permissions]

Significance of detection of extra metacentric microchromosome in amniotic cell culture.
R Bernstein, C Hakim, B Hardwick, and G T Nurse
J Med Genet 1978; 15: 136-142. doi:10.1136/jmg.15.2.136 [Abstract] [PDF] [Request Permissions]

Partial trisomy for short and long arm of chromosome no. 5: Two cases of two possible syndromes.
B Zabel, W Baumann, J Gehler, and G Conrad
J Med Genet 1978; 15: 143-147. doi:10.1136/jmg.15.2.143 [Abstract] [PDF] [Request Permissions]

Partial trisomy 18 in a family with a translocation (18;21)(q21;q22).
M Niazi, D V Coleman, and P Saldaña-Garcia
J Med Genet 1978; 15: 148-151. doi:10.1136/jmg.15.2.148 [Abstract] [PDF] [Request Permissions]

De novo simultaneous reciprocal translocation and deletion.
K Fries, G Mundel, and M Rosenblatt
J Med Genet 1978; 15: 152-154. doi:10.1136/jmg.15.2.152 [Abstract] [PDF] [Request Permissions]

Y autosome translocation and complex chromosome rearrangement in cri du chat syndrome.
J F Mattei, M G Mattei, J Coignet, and F Giraud
J Med Genet 1978; 15: 154-157. doi:10.1136/jmg.15.2.154 [Abstract] [PDF] [Request Permissions]

Erythropoietic protoporphyria, heterozygous cystinuria, and reduced peptidase A activity in a patient with 46,XX/46,XX,18q--mosaicism.
E W Naylor, W H Murphey, E I Domoszlai, and R Guthrie
J Med Genet 1978; 15: 157-160. doi:10.1136/jmg.15.2.157 [Abstract] [PDF] [Request Permissions]

Familial radioulnar synostosis.
R A Spritz
J Med Genet 1978; 15: 160-162. doi:10.1136/jmg.15.2.160 [Abstract] [PDF] [Request Permissions]

Cleft palate and accessory metacarpal of index finger syndrome: possible familial occurrence.
M Gewitz, R Dinwiddie, T Yuille, F Hill, and C O Carter
J Med Genet 1978; 15: 162-164. doi:10.1136/jmg.15.2.162 [Abstract] [PDF] [Request Permissions]

Register for free content

The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.

Genetics jobs

Show me all >>

	A family study of vesicoureteric reflux Aida De Vargas, Kathleen Evans, P. Ransley, A. R. Rosenberg, D. Rothwell, T. Sherwood, D. I. Williams, T. M. Barratt, and C. O. Carter J Med Genet 1978; 15: 85-96. doi:10.1136/jmg.15.2.85 [Abstract] [PDF] [Request Permissions]

	Cellular content of amniotic fluid as predictor of central nervous system malformations. M Bobrow, C J Evans, J Noble, and C Patel J Med Genet 1978; 15: 97-100. doi:10.1136/jmg.15.2.97 [Abstract] [PDF] [Request Permissions]

	Shifting genetic patterns in anencephaly and spina bifida. D T Janerich and J Piper J Med Genet 1978; 15: 101-105. doi:10.1136/jmg.15.2.101 [Abstract] [PDF] [Request Permissions]

	Use of overlapping normal distributions in genetic counselling. N R Dennis and C O Carter J Med Genet 1978; 15: 106-108. doi:10.1136/jmg.15.2.106 [Abstract] [PDF] [Request Permissions]

	Genetic counseling of consanguineous families. Use of Smith's method to calculate recurrence risks in multifactorial inheritance in consanguineous matings. C Bonaiti J Med Genet 1978; 15: 109-112. doi:10.1136/jmg.15.2.109 [Abstract] [PDF] [Request Permissions]

	Linkage relations of a locus for congenital total nuclear cataract. R S Huntzinger, L R Weitkamp, and P D Roca J Med Genet 1978; 15: 113-115. doi:10.1136/jmg.15.2.113 [Abstract] [PDF] [Request Permissions]

	Unusual inheritance of Becker type muscular dystrophy. L Aguilar, R Lisker, and G G Ramos J Med Genet 1978; 15: 116-118. doi:10.1136/jmg.15.2.116 [Abstract] [PDF] [Request Permissions]

	Hereditary brachydactyly with nail dysplasia. G D Schott J Med Genet 1978; 15: 119-122. doi:10.1136/jmg.15.2.119 [Abstract] [PDF] [Request Permissions]

	Recessively inherited costovertebral segmentation defect with mesomelia and peculiar facies (Covesdem syndrome): A new genetic entity? R S Wadia, D B Shirole, and M S Dikshit J Med Genet 1978; 15: 123-127. doi:10.1136/jmg.15.2.123 [Abstract] [PDF] [Request Permissions]

	A new type of chondrodystrophic mutant in the mouse. J M Ferguson, M E Wallace, and D R Johnson J Med Genet 1978; 15: 128-131. doi:10.1136/jmg.15.2.128 [Abstract] [PDF] [Request Permissions]

	Fertility in 47,XXX and 45,X patients. J Dewhurst J Med Genet 1978; 15: 132-135. doi:10.1136/jmg.15.2.132 [Abstract] [PDF] [Request Permissions]

	Significance of detection of extra metacentric microchromosome in amniotic cell culture. R Bernstein, C Hakim, B Hardwick, and G T Nurse J Med Genet 1978; 15: 136-142. doi:10.1136/jmg.15.2.136 [Abstract] [PDF] [Request Permissions]

	Partial trisomy for short and long arm of chromosome no. 5: Two cases of two possible syndromes. B Zabel, W Baumann, J Gehler, and G Conrad J Med Genet 1978; 15: 143-147. doi:10.1136/jmg.15.2.143 [Abstract] [PDF] [Request Permissions]

	Partial trisomy 18 in a family with a translocation (18;21)(q21;q22). M Niazi, D V Coleman, and P Saldaña-Garcia J Med Genet 1978; 15: 148-151. doi:10.1136/jmg.15.2.148 [Abstract] [PDF] [Request Permissions]

	De novo simultaneous reciprocal translocation and deletion. K Fries, G Mundel, and M Rosenblatt J Med Genet 1978; 15: 152-154. doi:10.1136/jmg.15.2.152 [Abstract] [PDF] [Request Permissions]

	Y autosome translocation and complex chromosome rearrangement in cri du chat syndrome. J F Mattei, M G Mattei, J Coignet, and F Giraud J Med Genet 1978; 15: 154-157. doi:10.1136/jmg.15.2.154 [Abstract] [PDF] [Request Permissions]

	Erythropoietic protoporphyria, heterozygous cystinuria, and reduced peptidase A activity in a patient with 46,XX/46,XX,18q--mosaicism. E W Naylor, W H Murphey, E I Domoszlai, and R Guthrie J Med Genet 1978; 15: 157-160. doi:10.1136/jmg.15.2.157 [Abstract] [PDF] [Request Permissions]

	Familial radioulnar synostosis. R A Spritz J Med Genet 1978; 15: 160-162. doi:10.1136/jmg.15.2.160 [Abstract] [PDF] [Request Permissions]

	Cleft palate and accessory metacarpal of index finger syndrome: possible familial occurrence. M Gewitz, R Dinwiddie, T Yuille, F Hill, and C O Carter J Med Genet 1978; 15: 162-164. doi:10.1136/jmg.15.2.162 [Abstract] [PDF] [Request Permissions]