Authors:
Lewis, Cathryn M.
Levinson, Douglas F.
Wise, Lesley H.
DeLisi, Lynn E.
Straub, Richard E.
Hovatta, Iiris
Williams, Nigel M.
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Pulver, Ann E.
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Brzustowicz, Linda M.
Kaufmann, Charles A.
Garver, David L.
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Lindholm, Eva
Coon, Hilary
Moises, Hans W.
Byerley, William
Shaw, Sarah H.
Mesen, Andrea
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Walsh, Dermot
Kendler, Kenneth S.
Ekelund, Jesper
Paunio, Tiina
Lönnqvist, Jouko
Peltonen, Leena
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Wildenauer, Dieter B.
Maier, Wolfgang
Nestadt, Gerald
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Antonarakis, Stylianos E.
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Malaspina, Dolores
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Sigmundsson, Thordur
Petursson, Hannes
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Zoëga, Tomas
Helgason, Tomas
Citation: M. Lewis, Cathryn et al., Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia, American journal of human genetics , 73(1), 2003, pp. 34-48
Authors:
Petersen, Michael B.
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Citation: B. Petersen, Michael et al., Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndrome., American journal of human genetics , 48-I(1), 1991, pp. 65-71
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Naveed, Mohammed
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Gaines, Mathew
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Radhakrishna, Uppala
Citation: Naveed, Mohammed et al., Genomewide Linkage Scan for Split.Hand/Foot Malformation with Long-Bone Deficiency in a Large Arab Family Identifies Two Novel Susceptibility Loci on Chromosomes 1q42.2-q43 and 6q14.1, American journal of human genetics , 80(1), 2007, pp. 105-111
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Prandini, Paola
Deutsch, Samuel
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Delucinge Vivier, Celine
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Gehrig, Corinne
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Baldo, Chiara
Novelli, Antonio
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Citation: Prandini, Paola et al., Natural Gene-Expression Variation in Down Syndrome Modulates the Outcome of Gene-Dosage Imbalance, American journal of human genetics , 81(2), 2007, pp. 252-263
Authors:
Cutting, Gary R.
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Kasch, Laura M.
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Citation: R. Cutting, Gary et al., Analysis of dna polymorphism haplotypes linked to the cystic fibrosis locus in north american black and caucasian families supports the existence of multiple mutations of the cystic fibrosis gene, American journal of human genetics , 44(3), 1989, pp. 307-318
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Merla, Giuseppe
Howald, Cédric
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Citation: Merla, Giuseppe et al., Submicroscopic Deletion in Patients with Williams-Beuren Syndrome Influences Expression Levels of the Nonhemizygous Flanking Genes, American journal of human genetics , 79(2), 2006, pp. 332-341
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Anagnou, Nicholas P.
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Citation: P. Anagnou, Nicholas et al., Chromosomal localization and racial distribution of the polymorphic human dihydrofolate reductase pseudogene (DHFRPI), American journal of human genetics , 42(2), 1988, pp. 345-352
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Citation: B. Petersen, Michael et al., Down syndrome due to de novo Robertsonian translocation t(14q;21q): DNA polymorphism analysis suggests that the origin of the extra 21q is maternal., American journal of human genetics , 49-I(3), 1991, pp. 529-536
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Antonarakis, Stylianos E.
Petersen, Michael B.
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Adelsberger, Patricia A.
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Raoul, Odile
Slaugenhaupt, Susan A.
Hafez, Mohamed
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Roulson, Diane
Schwartz, Stuart
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Tranebjaerg, Lisbeth
Greenberg, Frank
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Chakravarti, Aravinda
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Bowden, Donald W.
Akots, Gita
Rothschild, Cynthia B.
Falls, Kathleen F.
Sheehy, Michael J.
Hayward, Caroline
Mackie, Alisdair
Baird, Joyce
Brock, David
Antonarakis, Stylianos E.
Fajans, Stefan S.
Citation: W. Bowden, Donald et al., Linkage analysis of maturity-onset diabetes of the young (MODY): Genetic heterogeneity and nonpenetrance, American journal of human genetics , 50-I(3), 1992, pp. 607-618
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Youssoufian, Hagop
Antonarakis, Stylianos E.
Bell, William
Griffin, Anne M.
Kazazian, Haig H.
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Citation: Youssoufian, Hagop et al., Nonsense and Missense Mutations in Hemophilia A: Estimate of the Relative Mutation Rate at CG Dinucleotides, American journal of human genetics , 42(5), 1988, pp. 718-725
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Ferrari, Serge L.
Deutch, Samuel
Choudhury, Urmila
Chevalley, Thierry
Bonjour, Jean-Philippe
Dermitzakis, Emmanouil T.
Rizzoli, René
Antonarakis, Stylianos E.
Citation: L. Ferrari, Serge et al., Polymorphisms in the Low-Density Lipoprotein Receptor.Related Protein 5 (LRP5) Gene Are Associated with Variation in Vertebral Bone Mass, Vertebral Bone Size, and Stature in Whites, American journal of human genetics , 74(5), 2004, pp. 866-875
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Youssoufian, Hagop
Wong, Corinne
Aronis, Sophia
Platokoukis, Helen
Kazazian, Haig H.
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Citation: Youssoufian, Hagop et al., Moderately severe hemophilia A resulting from Glu-.Gly substitution in exon 7 of the factor VIll gene, American journal of human genetics , 42(6), 1988, pp. 867-871
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Antonarakis, Stylianos E.
Adelsberger, Patricia A.
Petersen, Michael B.
Binkert, Franz
Schinzel, Albert A.
Citation: E. Antonarakis, Stylianos et al., Analysis of DNA polymorphisms suggests that most de novo dup(21q) chromosomes in patients with Down syndrome are isochromosomes and not translocations., American journal of human genetics , 47-II(6), 1990, pp. 968-972
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Coresh, Josef
Beaty, Terri H.
Kwiterovich, Peter O. Jr
Antonarakis, Stylianos E.
Citation: Coresh, Josef et al., Pedigree and sib-pair linkage analysis suggest the apolipoprotein B gene is not the major gene influencing plasma apolipoprotein B levels., American journal of human genetics , 50-II(5), 1992, pp. 1038-1045