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Volume 48(5);  1991 May

The cover of the journal

Research on DNA typing catching up with courtroom application.
E S Lander
Am J Hum Genet. 1991 May; 48(5): 819–823.
PMCID:
PMC1683053
Summary Page Browse PDF–800KCite
The efficiency of multilocus DNA fingerprint probes for individualization and establishment of family relationships, determined from extensive casework.
A J Jeffreys, M Turner, P Debenham
Am J Hum Genet. 1991 May; 48(5): 824–840.
PMCID:
PMC1683038
Summary Page Browse PDF–3.1MCite
Fixed-bin analysis for statistical evaluation of continuous distributions of allelic data from VNTR loci, for use in forensic comparisons.
B Budowle, A M Giusti, J S Waye, F S Baechtel, R M Fourney, D E Adams, L A Presley, H A Deadman, K L Monson
Am J Hum Genet. 1991 May; 48(5): 841–855.
PMCID:
PMC1683046
Summary Page Browse PDF–2.0MCite
Cytogenetic analysis of sperm from a man heterozygous for a pericentric inversion, inv (3) (p25q21).
R H Martin
Am J Hum Genet. 1991 May; 48(5): 856–861.
PMCID:
PMC1683062
Summary Page Browse PDF–1.3MCite
Use of the robust sib-pair method to screen for single-locus, multiple-locus, and pleiotropic effects: application to traits related to hypertension.
A F Wilson, R C Elston, L D Tran, R M Siervogel
Am J Hum Genet. 1991 May; 48(5): 862–872.
PMCID:
PMC1683060
Summary Page Browse PDF–1.6MCite
Atopic disease and immunoglobulin E in twins reared apart and together.
B Hanson, M McGue, B Roitman-Johnson, N L Segal, T J Bouchard, Jr, M N Blumenthal
Am J Hum Genet. 1991 May; 48(5): 873–879.
PMCID:
PMC1683042
Summary Page Browse PDF–913KCite
Allele-specific hypermethylation of the retinoblastoma tumor-suppressor gene.
T Sakai, J Toguchida, N Ohtani, D W Yandell, J M Rapaport, T P Dryja
Am J Hum Genet. 1991 May; 48(5): 880–888.
PMCID:
PMC1683063
Summary Page Browse PDF–1.8MCite
Structure of the chromosomal gene and cDNAs coding for lactase-phlorizin hydrolase in humans with adult-type hypolactasia or persistence of lactase.
W Boll, P Wagner, N Mantei
Am J Hum Genet. 1991 May; 48(5): 889–902.
PMCID:
PMC1683064
Summary Page Browse PDF–2.5MCite
Extended haplotypes and linkage disequilibrium between 11 markers at the APOA1-C3-A4 gene cluster on chromosome 11
P. Benlian, C. Boileau, N. Loux, D. Pastier, J. Masliah, M. Coulon, M. Nigou, A. Ragab, J. Guimard, J. B. Ruidavets, C. Bonaïti-Pellié, J. C. Fruchart, P. Douste-Blazy, G. Bereziat, C. Junien
Am J Hum Genet. 1991 May; 48(5): 903–910.
PMCID:
PMC1683058
Summary Page Browse PDF–1.1MCite
A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates
Kenneth H. Buetow, Rita Shiang, Ping Yang, Yusuke Nakamura, G. Mark Lathrop, Raymond White, John J. Wasmuth, Stephen Wood, Laura D. Berdahl, Nancy J. Leysens, Timothy M. Ritty, Molly E. Wise, Jeffrey C. Murray
Am J Hum Genet. 1991 May; 48(5): 911–925.
PMCID:
PMC1683054
Summary Page Browse PDF–1.9MCite
Testing for association between disease and linked marker loci: a log-linear-model analysis.
L Tiret, P Amouyel, R Rakotovao, F Cambien, P Ducimetière
Am J Hum Genet. 1991 May; 48(5): 926–934.
PMCID:
PMC1683048
Summary Page Browse PDF–1.2MCite
Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation.
N Howell, I Kubacka, M Xu, D A McCullough
Am J Hum Genet. 1991 May; 48(5): 935–942.
PMCID:
PMC1683051
Summary Page Browse PDF–1.3MCite
Deletion of the entire cytochrome P450 CYP2D6 gene as a cause of impaired drug metabolism in poor metabolizers of the debrisoquine/sparteine polymorphism.
A Gaedigk, M Blum, R Gaedigk, M Eichelbaum, U A Meyer
Am J Hum Genet. 1991 May; 48(5): 943–950.
PMCID:
PMC1683061
Summary Page Browse PDF–1.3MCite
Identification of 17 independent mutations responsible for human hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency.
B L Davidson, S A Tarlé, M Van Antwerp, D A Gibbs, R W Watts, W N Kelley, T D Palella
Am J Hum Genet. 1991 May; 48(5): 951–958.
PMCID:
PMC1683055
Summary Page Browse PDF–1.7MCite
Evidence for the segregation of a major gene in human susceptibility/resistance to infection by Schistosoma mansoni.
L Abel, F Demenais, A Prata, A E Souza, A Dessein
Am J Hum Genet. 1991 May; 48(5): 959–970.
PMCID:
PMC1683050
Summary Page Browse PDF–1.9MCite
Identification of a mutation in the arylsulfatase A gene of a patient with adult-type metachromatic leukodystrophy.
R Kondo, N Wakamatsu, H Yoshino, N Fukuhara, T Miyatake, S Tsuji
Am J Hum Genet. 1991 May; 48(5): 971–978.
PMCID:
PMC1683039
Summary Page Browse PDF–1.1MCite
Proline at position 36: a new transthyretin mutation associated with familial amyloidotic polyneuropathy.
L A Jones, J C Skare, J A Harding, A S Cohen, A Milunsky, M Skinner
Am J Hum Genet. 1991 May; 48(5): 979–982.
PMCID:
PMC1683065
Summary Page Browse PDF–778KCite
2,8-Dihydroxyadenine lithiasis in a Japanese patient heterozygous at the adenine phosphoribosyltransferase locus.
A Sahota, J Chen, M A Behzadian, R Ravindra, H Takeuchi, P J Stambrook, J A Tischfield
Am J Hum Genet. 1991 May; 48(5): 983–989.
PMCID:
PMC1683049
Summary Page Browse PDF–1.1MCite
Chromosomal assignments of the human endothelin family genes: the endothelin-1 gene (EDN1) to 6p23-p24, the endothelin-2 gene (EDN2) to 1p34, and the endothelin-3 gene (EDN3) to 20q13.2-q13.3.
T Arinami, M Ishikawa, A Inoue, M Yanagisawa, T Masaki, M C Yoshida, H Hamaguchi
Am J Hum Genet. 1991 May; 48(5): 990–996.
PMCID:
PMC1683044
Summary Page Browse PDF–1.0MCite
Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT.
V Huff, H Miwa, D A Haber, K M Call, D Housman, L C Strong, G F Saunders
Am J Hum Genet. 1991 May; 48(5): 997–1003.
PMCID:
PMC1683037
Summary Page Browse PDF–1.0MCite
Molecular analyses of an acidic transthyretin Asn 90 variant.
M J Saraiva, M R Almeida, I L Alves, P Moreira, M Gawinowicz, P P Costa, S Rauh, A Banhzoff, K Altland
Am J Hum Genet. 1991 May; 48(5): 1004–1008.
PMCID:
PMC1683057
Summary Page Browse PDF–870KCite
American Society of Human Genetics Social Issues Committee report on genetics and adoption: points to consider.
Am J Hum Genet. 1991 May; 48(5): 1009–1010.
PMCID:
PMC1683047
Summary Page Browse PDF–220KCite
American Society of Human Genetics statement on clinical genetics and freedom of choice.
Am J Hum Genet. 1991 May; 48(5): 1011.
PMCID:
PMC1683059
Summary Page Browse PDF–83KCite
Further evidence for an association between genetic variation in transforming growth factor alpha and cleft lip and palate.
G Chenevix-Trench, K Jones, A Green, N Martin
Am J Hum Genet. 1991 May; 48(5): 1012–1013.
PMCID:
PMC1683066
Summary Page Browse PDF–271KCite
Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.
R Happle
Am J Hum Genet. 1991 May; 48(5): 1013–1014.
PMCID:
PMC1683040
Summary Page Browse PDF–323KCite
Different clinical manifestations of hyperphenylalaninemia in three siblings with identical phenylalanine hydroxylase genes.
D DiSilvestre, R Koch, J Groffen
Am J Hum Genet. 1991 May; 48(5): 1014–1016.
PMCID:
PMC1683043
Summary Page Browse PDF–620KCite

Correction

Erratum
Am J Hum Genet. 1991 May; 48(5): 1017.
Corrects:
Am J Hum Genet. 1991 Feb; 48(2): 325–334.
PMCID:
PMC1683056
Correction PDF–17KCite

Journal Matter

Original table of contents page
PDF–198K
Administrative content — journal masthead, notices, indexes, etc.
PDF–1.7M
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PDF–988K
Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics