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                             22 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A Constrained-Likelihood Approach to Marker-Trait Association Studies Wang, Kai
2005
77 5 p. 768-780
13 p.
artikel
2 Announcements 1 1.  Announcements are published free of charge for members of The American Society of Human Genetics (ASHG). Please e-mail announcements to ajhg@ajhg.net. Submission must be received at least 7 weeks before the month of issue in which publication is requested. They must be double spaced with a 1½-inch margin on all sides. The maximum length is 250 words, excluding the address for correspondence. Please include a cover letter indicating the name of the sponsoring ASHG member. 2005
77 5 p. 899-901
3 p.
artikel
3 A Novel Method with Improved Power To Detect Recombination Hotspots from Polymorphism Data Reveals Multiple Hotspots in Human Genes Fearnhead, Paul
2005
77 5 p. 781-794
14 p.
artikel
4 Children with Idiopathic Hemihypertrophy and Beckwith-Wiedemann Syndrome Have Different Constitutional Epigenotypes Associated with Wilms Tumor Niemitz, Emily L.
2005
77 5 p. 887-891
5 p.
artikel
5 Clinical and Molecular Findings in Osteoporosis-Pseudoglioma Syndrome Ai, Minrong
2005
77 5 p. 741-753
13 p.
artikel
6 Curcumin Treatment Abrogates Endoplasmic Reticulum Retention and Aggregation-Induced Apoptosis Associated with Neuropathy-Causing Myelin Protein Zero–Truncating Mutants Khajavi, Mehrdad
2005
77 5 p. 841-850
10 p.
artikel
7 Erratum 2005
77 5 p. 898-
1 p.
artikel
8 Evidence for Widespread Reticulate Evolution within Human Duplicons Jackson, Michael S.
2005
77 5 p. 824-840
17 p.
artikel
9 Genetic Disorders and the Fetus: Diagnosis, Prevention and Treatment. Bennett, Robin L.
2005
77 5 p. 896-
1 p.
artikel
10 Genetics of Developmental Disabilities. Vekemans, Michel
2005
77 5 p. 896-897
2 p.
artikel
11 Handling Marker-Marker Linkage Disequilibrium: Pedigree Analysis with Clustered Markers Abecasis, Gonçalo R.
2005
77 5 p. 754-767
14 p.
artikel
12 High-Resolution Identification of Chromosomal Abnormalities Using Oligonucleotide Arrays Containing 116,204 SNPs Slater, Howard R.
2005
77 5 p. 709-726
18 p.
artikel
13 High-Resolution Whole-Genome Association Study of Parkinson Disease Maraganore, Demetrius M.
2005
77 5 p. 685-693
9 p.
artikel
14 Multiple Correcting COL17A1 Mutations in Patients with Revertant Mosaicism of Epidermolysis Bullosa Pasmooij, Anna M.G.
2005
77 5 p. 727-740
14 p.
artikel
15 Mutations in TCF8 Cause Posterior Polymorphous Corneal Dystrophy and Ectopic Expression of COL4A3 by Corneal Endothelial Cells Krafchak, Charles M.
2005
77 5 p. 694-708
15 p.
artikel
16 Narrowing the Candidate Region for Congenital Diaphragmatic Hernia in Chromosome 15q26: Contradictory Results Castiglia, L.
2005
77 5 p. 892-894
3 p.
artikel
17 Promoter and 3′-Untranslated-Region Haplotypes in the Vitamin D Receptor Gene Predispose to Osteoporotic Fracture: The Rotterdam Study Fang, Yue
2005
77 5 p. 807-823
17 p.
artikel
18 Reply to Castiglia et al. Klaassens, M.
2005
77 5 p. 894-895
2 p.
artikel
19 Severely Incapacitating Mutations in Patients with Extreme Short Stature Identify RNA-Processing Endoribonuclease RMRP as an Essential Cell Growth Regulator Thiel, Christian T.
2005
77 5 p. 795-806
12 p.
artikel
20 Support for the Homeobox Transcription Factor Gene ENGRAILED 2 as an Autism Spectrum Disorder Susceptibility Locus Benayed, Rym
2005
77 5 p. 851-868
18 p.
artikel
21 The Heritage of Pathogen Pressures and Ancient Demography in the Human Innate-Immunity CD209/CD209L Region Barreiro, Luis B.
2005
77 5 p. 869-886
18 p.
artikel
22 This Month in the Journal Garber, Kathryn
2005
77 5 p. i-ii
nvt p.
artikel
                             22 gevonden resultaten
 
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