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Volume 45(2);  1989 Aug

The cover of the journal

Of mice, persons, and pigment.
B D Hall
Am J Hum Genet. 1989 Aug; 45(2): 191–192.
PMCID:
PMC1683361
Summary Page Browse PDF–193K
Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.
I T Thomas, J L Frias, E S Cantu, C Z Lafer, D B Flannery, J G Graham, Jr
Am J Hum Genet. 1989 Aug; 45(2): 193–205.
PMCID:
PMC1683341
Summary Page Browse PDF–2.0M
Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism.
J Vilkki, M L Savontaus, E K Nikoskelainen
Am J Hum Genet. 1989 Aug; 45(2): 206–211.
PMCID:
PMC1683352
Summary Page Browse PDF–820K
Gaucher disease: molecular heterogeneity and phenotype-genotype correlations.
B Theophilus, T Latham, G A Grabowski, F I Smith
Am J Hum Genet. 1989 Aug; 45(2): 212–225.
PMCID:
PMC1683351
Summary Page Browse PDF–2.6M
Analyzing the relationship between age at onset and risk to relatives.
M C Neale, L J Eaves, J K Hewitt, C J MacLean, J M Meyer, K S Kendler
Am J Hum Genet. 1989 Aug; 45(2): 226–239.
PMCID:
PMC1683360
Summary Page Browse PDF–2.3M
Cardiovascular risk factors in a French-Canadian population: resolution of genetic and familial environmental effects on blood pressure by using extensive information on environmental correlates.
L Pérusse, T Rice, C Bouchard, G P Vogler, D C Rao
Am J Hum Genet. 1989 Aug; 45(2): 240–251.
PMCID:
PMC1683357
Summary Page Browse PDF–1.6M
Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RB1 gene.
H Scheffer, G J te Meerman, Y C Kruize, A H van den Berg, D P Penninga, K E Tan, D J der Kinderen, C H Buys
Am J Hum Genet. 1989 Aug; 45(2): 252–260.
Correction in:
Am J Hum Genet. 1989 Dec; 45(6): 983.
PMCID:
PMC1683338
Summary Page Browse PDF–1.4M
Genetic analysis of HLA in the U.S. Schmiedenleut Hutterites.
D D Kostyu, C L Ober, D V Dawson, M Ghanayem, S Elias, A O Martin
Am J Hum Genet. 1989 Aug; 45(2): 261–269.
PMCID:
PMC1683340
Summary Page Browse PDF–1.0M
ATFresno: a phenotype linking ataxia-telangiectasia with the Nijmegen breakage syndrome.
C J Curry, P O'Lague, J Tsai, H T Hutchison, N G Jaspers, D Wara, R A Gatti, H T Hutchinson
Am J Hum Genet. 1989 Aug; 45(2): 270–275.
Correction in:
Am J Hum Genet. 1989 Oct; 45(4): 663.
PMCID:
PMC1683342
Summary Page Browse PDF–829K
Assignment of human genes for phosphorylase kinase subunits alpha (PHKA) to Xq12-q13 and beta (PHKB) to 16q12-q13.
U Francke, B T Darras, N F Zander, M W Kilimann
Am J Hum Genet. 1989 Aug; 45(2): 276–282.
PMCID:
PMC1683359
Summary Page Browse PDF–988K
Genomic organization of the human asparagine transfer RNA genes: localization to the U1 RNA gene and class I pseudogene repeat units.
R A Buckland
Am J Hum Genet. 1989 Aug; 45(2): 283–295.
PMCID:
PMC1683362
Summary Page Browse PDF–3.5M
Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5.
J Overhauser, U Bengtsson, J McMahon, J Ulm, M G Butler, L Santiago, J J Wasmuth
Am J Hum Genet. 1989 Aug; 45(2): 296–303.
PMCID:
PMC1683354
Summary Page Browse PDF–1.4M
Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304).
N Dahl, P Goonewardena, H Malmgren, K H Gustavson, G Holmgren, E Seemanova, G Annerén, A Flood, U Pettersson
Am J Hum Genet. 1989 Aug; 45(2): 304–309.
PMCID:
PMC1683358
Summary Page Browse PDF–847K
Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in European families with phenylketonuria (PKU)
Stephen P. Daiger, Ranajit Chakraborty, Lori Reed, György Fekete, Dezso Schuler, György Berenssi, Istvan Nasz, Radim Brdička, Jaromir Kamarýt, Anna Pijáčková, Sharon Moore, Susan Sullivan, Savio L. C. Woo
Am J Hum Genet. 1989 Aug; 45(2): 310–318.
PMCID:
PMC1683346
Summary Page Browse PDF–1.2M
Polymorphic DNA haplotypes at the phenlalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU)
Stephen P. Daiger, Lori Reed, Shu-Shen Huang, Yi-Tao Zeng, Tao Wang, Wilson H. Y. Lo, Yoshiyuki Okano, Yutaka Hase, Y. Fukuda, Toshiaki Oura, Keiya Tada, Savio L. C. Woo
Am J Hum Genet. 1989 Aug; 45(2): 319–324.
PMCID:
PMC1683348
Summary Page Browse PDF–830K
Detection of an amino acid substitution in the mutant enzyme for a special type of adenine phosphoribosyltransferase (APRT) deficiency by sequence-specific protein cleavage.
N Kamatani, S Kuroshima, C Terai, Y Hidaka, T D Palella, K Nishioka
Am J Hum Genet. 1989 Aug; 45(2): 325–331.
PMCID:
PMC1683345
Summary Page Browse PDF–1.4M
Update on MSAFP policy statement from the American Society of Human Genetics.
K L Garver
Am J Hum Genet. 1989 Aug; 45(2): 332–334.
PMCID:
PMC1683337
Summary Page Browse PDF–353K
Methylation at the Huntington disease-linked D4S95 locus.
C A Pritchard, D R Cox, R M Myers
Am J Hum Genet. 1989 Aug; 45(2): 335–336.
PMCID:
PMC1683353
Summary Page Browse PDF–285K
Glasnost and Perestroika in human genetics.
L L Cavalli-Sforza
Am J Hum Genet. 1989 Aug; 45(2): 336–337.
PMCID:
PMC1683344
Summary Page Browse PDF–348K
A PCR artifact: generation of heteroduplexes.
C M Nagamine, K Chan, Y F Lau
Am J Hum Genet. 1989 Aug; 45(2): 337–339.
PMCID:
PMC1683350
Summary Page Browse PDF–489K

Book Reviews

Molecular biology of the eye, vol. 88: Genes, vision, and ocular disease
P. J. Ringens, P. R. Cotran
Am J Hum Genet. 1989 Aug; 45(2): 340.
PMCID:
PMC1683347
Summary Page Browse PDF–115K
Choices, not chances
Victoria A. Cox
Am J Hum Genet. 1989 Aug; 45(2): 340–341.
PMCID:
PMC1683355
Summary Page Browse PDF–312K

Correction

Erratum
Am J Hum Genet. 1989 Aug; 45(2): 342.
Corrects:
Am J Hum Genet. 1989 May; 44(5): 695–703.
PMCID:
PMC1683339
Correction PDF–13K

Journal Matter

Original table of contents page
PDF–158K
Administrative content — journal masthead, notices, indexes, etc.
PDF–993K
Advertisements
PDF–480K
Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics
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