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Volume 41(4);  1987 Oct

The cover of the journal

A genetical model for emergenesis: in memory of Laurence H. Snyder, 1901-86.
C C Li
Am J Hum Genet. 1987 Oct; 41(4): 517–523.
PMCID:
PMC1684313
Summary Page Browse PDF–700K
Spinocerebellar ataxia: localization of an autosomal dominant locus between two markers on human chromosome 6.
S S Rich, P Wilkie, L Schut, G Vance, H T Orr
Am J Hum Genet. 1987 Oct; 41(4): 524–531.
PMCID:
PMC1684306
Summary Page Browse PDF–702K
Tay-Sachs disease with hexosaminidase A: characterization of the defective enzyme in two patients.
J Bayleran, P Hechtman, E Kolodny, M Kaback
Am J Hum Genet. 1987 Oct; 41(4): 532–548.
PMCID:
PMC1684329
Summary Page Browse PDF–1.4M
The economics of clinical genetics services. I. Preview.
R E Pyeritz, J E Tumpson, B A Bernhardt
Am J Hum Genet. 1987 Oct; 41(4): 549–558.
PMCID:
PMC1684311
Summary Page Browse PDF–1.0M
The economics of clinical genetics services. II. A time analysis of a medical genetics clinic.
B A Bernhardt, J Weiner, E C Foster, J E Tumpson, R E Pyeritz
Am J Hum Genet. 1987 Oct; 41(4): 559–565.
PMCID:
PMC1684316
Summary Page Browse PDF–780K
Association of congenital deficiency of multiple vitamin K-dependent coagulation factors and the phenotype of the warfarin embryopathy: clues to the mechanism of teratogenicity of coumarin derivatives.
R M Pauli, J B Lian, D F Mosher, J W Suttie
Am J Hum Genet. 1987 Oct; 41(4): 566–583.
PMCID:
PMC1684308
Summary Page Browse PDF–2.1M
Abnormal kinetic behavior of cytochrome oxidase in a case of Leigh disease.
M Glerum, B H Robinson, C Spratt, J Wilson, D Patrick
Am J Hum Genet. 1987 Oct; 41(4): 584–593.
PMCID:
PMC1684310
Summary Page Browse PDF–983K
An XXX male resulting from paternal X-Y interchange and maternal X-X nondisjunction.
G Annerén, M Andersson, D C Page, L G Brown, M Berg, G Läckgren, K H Gustavson, A de la Chapelle
Am J Hum Genet. 1987 Oct; 41(4): 594–604.
PMCID:
PMC1684314
Summary Page Browse PDF–2.0M
Isolation of a cDNA clone for the human laminin-B1 chain and its gene localization.
M Jaye, W S Modi, G A Ricca, R Mudd, I M Chiu, S J O'Brien, W N Drohan
Am J Hum Genet. 1987 Oct; 41(4): 605–615.
PMCID:
PMC1684322
Summary Page Browse PDF–1.5M
The gene encoding human vimentin is located on the short arm of chromosome 10.
S Ferrari, L A Cannizzaro, R Battini, K Huebner, R Baserga
Am J Hum Genet. 1987 Oct; 41(4): 616–626.
PMCID:
PMC1684315
Summary Page Browse PDF–1.5M
Linkage studies of Friedreich ataxia by means of blood-group and protein markers
B. J. B. Keats, L. J. Ward, M. Lu, S. Krieger, M. A. Wilensky, C. J. Forster-Gibson, M. Roy, M. Monté, A. Barbeau, N. E. Simpson, H. Eiberg, P. Tippett, R. Williamson, S. Chamberlain
Am J Hum Genet. 1987 Oct; 41(4): 627–634.
PMCID:
PMC1684323
Summary Page Browse PDF–691K
Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14.
A F Wright, S S Bhattacharya, J F Clayton, M Dempster, P Tippett, C M McKeown, M Jay, B Jay, A C Bird
Am J Hum Genet. 1987 Oct; 41(4): 635–644.
PMCID:
PMC1684318
Summary Page Browse PDF–1.0M
Genetic studies of low-abundance human plasma proteins. VI. Polymorphism of hemopexin.
M I Kamboh, R E Ferrell
Am J Hum Genet. 1987 Oct; 41(4): 645–653.
PMCID:
PMC1684324
Summary Page Browse PDF–974K
Human ferritin genes: chromosomal assignments and polymorphisms.
R A Gatti, R Shaked, T K Mohandas, W Salser
Am J Hum Genet. 1987 Oct; 41(4): 654–667.
PMCID:
PMC1684326
Summary Page Browse PDF–2.3M
Rapid karyotyping of neonates on the basis of data from cord blood.
I Garnham, G R Sutherland
Am J Hum Genet. 1987 Oct; 41(4): 668–670.
PMCID:
PMC1684319
Summary Page Browse PDF–474K
The effects of genetic screening and assortative mating on lethal recessive-allele frequencies and homozygote incidence.
R B Campbell
Am J Hum Genet. 1987 Oct; 41(4): 671–677.
PMCID:
PMC1684307
Summary Page Browse PDF–736K
Distribution of beta-thalassemia mutations in south China and their association with haplotypes.
V Chan, T K Chan, F F Chebab, D Todd
Am J Hum Genet. 1987 Oct; 41(4): 678–685.
PMCID:
PMC1684325
Summary Page Browse PDF–674K
Prenatal studies in a family with transcobalamin II deficiency.
J S Mayes, B Say, D L Marcus
Am J Hum Genet. 1987 Oct; 41(4): 686–687.
PMCID:
PMC1684321
Summary Page Browse PDF–212K
Likelihoods in pedigree analysis under sequential sampling.
E Thompson
Am J Hum Genet. 1987 Oct; 41(4): 687–689.
PMCID:
PMC1684328
Summary Page Browse PDF–312K
Merging autosomal dominance and recessivity.
G B Van Ommen
Am J Hum Genet. 1987 Oct; 41(4): 689–691.
PMCID:
PMC1684309
Summary Page Browse PDF–252K

Book Review

Pregnancy for older women
James D. Goldberg
Am J Hum Genet. 1987 Oct; 41(4): 692.
PMCID:
PMC1684312
Summary Page Browse PDF–86K

Journal Matter

Original table of contents page
PDF–168K
Administrative content — journal masthead, notices, indexes, etc.
PDF–1.1M
Advertisements
PDF–283K
Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics
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