Journal Articles: 1995

books | meeting abstracts | book chapters
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1995

F Apaydin, SM Leal , M Iber, T Kandogan, U Braendle, O Cura, H-P Zenner (1995)
"Nonsyndromic Genetik Isit me Kaybe (Nonsyndromic genetic hearing loss)",
Turk Otolarengolojii Arsivi 33, 151-154
S Chatkupt, FA Hol, YY Shugart , MPA Geurds, ES Stenroos, MR Koenigsberger, BGJ Hamel, WG Johnson, ECM Mariman (1995)
"Absence of linkage between familial neural tube defects and PAX3 gene",
Journal of Medical Genetics, 32, 200-204.
[abstract ]
V Brancolini, L Cremonesi, E Belloni, E Pappalardo, R Bordoni, M Seia, S Russo, R Padoan, A Giunta, M Ferrari (1995),
"Search for mutations in pancreatic sufficient cystic fibrosis Italian patients: detection of 90% of molecular defects and identification of three novel mutations",
Human Genetics, 96, 312-318
CSJ Fann, J Ott (1995)
"Parsimonious estimation of sex-specific map distances by stepwise maximum likelihood regression",
Genomics, 29, 571-575.
[abstract] [ Full Text (postscript) ]
C Gambacorti-Passerini, J Ott , A Bergen (1995),
"Human molecular genetics network" (correspondence),
New England Journal of Medicine, 333, 1573
H Kobayashi, L Baumbach, TC Matise, A Schiavi, F Greenberg, E Hoffman (1995)
"A gene for a severe lethal form of X-linked arthrogryposis (X-linked infantile spinal muscular atrophy) maps to human chromosome Xp113-q112,"
Human Molecular Genetics, 4(7): 1213-1216
[ Medline entry]
A Lazzarini, ES Stenroos, T Lehner, V McKoy, B Gold, MK McCormack, CS Reid, J Ott , WG Johnson (1995),
"Short tandem repeat polymorphism linkage studies in a New England family with X-linked mental retardation (MRX20)",
American Journal of Medical Genetics, 57, 552-557
SM Leal, J Ott (1995)
"Incorporating the variability of genotype-specific penetrance probabilities in the calculation of risk support intervals",
Genetic Epidemiology, 12,859-862.
[abstract]
TC Matise (1995)
"Genome scanning for complex disease genes using the transmission/disequilibrium test and haplotype-based haplotype relative risk",
Genetic Epidemiology, 12, 641-645.
[ abstract] [ Medline entry]
J Ott (1995)
"Linkage analysis with biological markers",
Human Heredity, 45, 169-174.
[abstract]
J Ott (1995)
"How do you compute a lod score?" (news and views),
Nature Genetics, 11, 354-355
D Pauls, J Ott , S M Paul, CR Allen, CJ Fann , JP Carulli, KM Falls, CA Bouthillier, TC Gravius, TP Keith, JA Egeland, EI Ginns (1995)
"Linkage analysis of chromosome 18 markers do not identify a major susceptibility locus for bipolar affected disorder in the old order Amish",
American Journal of Human Genetics, 57, 636-643.
[abstract]
AE Pulver, Lasseter VK, Kasch L, Wolyniec PS, Nestadt G, Blouin JL, Kimberland M, Babb R, Vourlis S, Chen H, Lalioti M, Morris MA, Karayiorgou M, J Ott, Meyers D, Antonarakis S, Housman D, Kazazian HH (1995),
"Schizophrenia: A genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes",
American Journal of Medical Genetics, 60, 252-260
MP Russo, G Romeo, M Devoto , G Barbujani, G Cabrini, A Giunta, E D'Alcamo, GB Leoni, F Sangiuolo, C Magnani, L Cremonesi, M Ferrari (1995)
"Analysis of linkage disequilibrium between different CF mutations and three intragenic microsatellites in the Italian population",
Human Mutation, 5, 23-27
YY Shugart , P Banerjee, JA Knowles, CA Lewis, SG Jacobson, TC Matise , G Penchaszadeh, T C Gilliam, J Ott (1995)
"Fine genetic mapping of a gene for autosomal recessive retinitis pigmentosa on chromosome 6p21",
American Journal of Human Genetics, 57(2), 499-502
YY Shugart (1995),
"Precision of marker heterozygosity estimates",
Genetic Epidemiology, 12,671-674
MC Speer, JD Terwilliger, J Ott (1995),
"Data simulation for GAW9 problems 1 and 2",
Genetic Epidemiology, 12: 561-564
[ Medline entry ]