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                             35 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A Fifth Locus for Bardet-Biedl Syndrome Maps to Chromosome 2q31 Young, Terry-Lynn
1999
64 3 p. 900-904
5 p.
artikel
2 A Genomewide Analysis Provides Evidence for Novel Linkages in Inflammatory Bowel Disease in a Large European Cohort Hampe, Jochen
1999
64 3 p. 808-816
9 p.
artikel
3 Analysis of Affected Sib Pairs, with Covariates—With and Without Constraints Greenwood, Celia M.T.
1999
64 3 p. 871-885
15 p.
artikel
4 Ancestral Asian Source(s) of New World Y-Chromosome Founder Haplotypes Karafet, T.M.
1999
64 3 p. 817-831
15 p.
artikel
5 Announcements 1 1.  Announcements are published free of charge for members of The American Society of Human Genetics (ASHG). Please send announcement text by E-mail to ajhg@u.washington.edu or by fax to (206) 685-9684. Please limit announcements to 150 words, excluding the address for correspondence, and indicate the name of the sponsoring ASHG member. Announcements will be posted on the electronic edition of the Journal within a week of receipt. For the print edition, submissions must be received 5 weeks before the month of the issue in which publication is requested. 1999
64 3 p. 916-917
2 p.
artikel
6 A Novel Skeletal Dysplasia with Developmental Delay and Acanthosis Nigricans Is Caused by a Lys650Met Mutation in the Fibroblast Growth Factor Receptor 3 Gene Tavormina, Patricia L.
1999
64 3 p. 722-731
10 p.
artikel
7 A Parametric Copula Model for Analysis of Familial Binary Data Trégouët, David-Alexandre
1999
64 3 p. 886-893
8 p.
artikel
8 Autosomal Dominant (Beukes) Premature Degenerative Osteoarthropathy of the Hip Joint Maps to an 11-cM Region on Chromosome 4q35 Roby, Philip
1999
64 3 p. 904-908
5 p.
artikel
9 Autosomal Dominant Myopathy with Proximal Weakness and Early Respiratory Muscle Involvement Maps to Chromosome 2q Nicolao, Piero
1999
64 3 p. 788-792
5 p.
artikel
10 Characterization and Mutation Analysis of Human LEFTY A and LEFTY B, Homologues of Murine Genes Implicated in Left-Right Axis Development Kosaki, K.
1999
64 3 p. 712-721
10 p.
artikel
11 Common Fragile Sites: G-Band Characteristics within an R-Band Mishmar, Dan
1999
64 3 p. 908-910
3 p.
artikel
12 Cyclic Ichthyosis with Epidermolytic Hyperkeratosis: A Phenotype Conferred by Mutations in the 2B Domain of Keratin K1 Sybert, Virginia P.
1999
64 3 p. 732-738
7 p.
artikel
13 Der(22) Syndrome and Velo-Cardio-Facial Syndrome/DiGeorge Syndrome Share a 1.5-Mb Region of Overlap on Chromosome 22q11 Funke, B.
1999
64 3 p. 747-758
12 p.
artikel
14 Diaphyseal Medullary Stenosis with Malignant Fibrous Histiocytoma: a Hereditary Bone Dysplasia/Cancer Syndrome Maps to 9p21-22 Martignetti, John A.
1999
64 3 p. 801-807
7 p.
artikel
15 Erratum 1999
64 3 p. 918-919
2 p.
artikel
16 Evidence for a Rare Prostate Cancer–Susceptibility Locus at Chromosome 1p36 Gibbs, Mark
1999
64 3 p. 776-787
12 p.
artikel
17 Evidence That Mutations in the X-linked DDP Gene Cause Incompletely Penetrant and Variable Skewed X Inactivation Plenge, Robert M.
1999
64 3 p. 759-767
9 p.
artikel
18 Finite-Sample Properties of Family-Based Association Tests Whittaker, J.C.
1999
64 3 p. 910-915
6 p.
artikel
19 Genomic Structure of the Canalicular Multispecific Organic Anion–Transporter Gene (MRP2/cMOAT) and Mutations in the ATP-Binding–Cassette Region in Dubin-Johnson Syndrome Toh, Satoshi
1999
64 3 p. 739-746
8 p.
artikel
20 Human Molybdopterin Synthase Gene: Genomic Structure and Mutations in Molybdenum Cofactor Deficiency Type B Reiss, J.
1999
64 3 p. 706-711
6 p.
artikel
21 Human Molybdopterin Synthase Gene: Identification of a Bicistronic Transcript with Overlapping Reading Frames Stallmeyer, B.
1999
64 3 p. 698-705
8 p.
artikel
22 Identifying Families with Likely Genetic Protective Factors against Alzheimer Disease Silverman, Jeremy M.
1999
64 3 p. 832-838
7 p.
artikel
23 Location Score and Haplotype Analyses of the Locus for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay, in Chromosome Region 13q11 Richter, Andrea
1999
64 3 p. 768-775
8 p.
artikel
24 Multipoint Oligogenic Analysis of Age-at-Onset Data with Applications to Alzheimer Disease Pedigrees Daw, E. Warwick
1999
64 3 p. 839-851
13 p.
artikel
25 Nitric Oxide in Endothelial Dysfunction and Vascular Remodeling: Clinical Correlates and Experimental Links Rudic, Radu D.
1999
64 3 p. 673-677
5 p.
artikel
26 Protein-Truncation Mutations in the RP2 Gene in a North American Cohort of Families with X-Linked Retinitis Pigmentosa Mears, Alan J.
1999
64 3 p. 897-900
4 p.
artikel
27 Psoriasis Linkage in the HLA Region Leder, Richard O.
1999
64 3 p. 895-
1 p.
artikel
28 Reply to Leder and Hodge Elder, James
1999
64 3 p. 896-897
2 p.
artikel
29 Specificity in Transforming Growth Factor–β Signaling Pathways Ring, C.J.
1999
64 3 p. 691-697
7 p.
artikel
30 Stress-Response Proteins in Cardiovascular Disease Xiao, XianZhong
1999
64 3 p. 685-690
6 p.
artikel
31 The Duty to Recontact: Attitudes of Genetics Service Providers Fitzpatrick, Jennifer L.
1999
64 3 p. 852-860
9 p.
artikel
32 The Molecular Basis of Vascular Disorders Towbin, Jeffrey A.
1999
64 3 p. 678-684
7 p.
artikel
33 The Predisposition to Type 1 Diabetes Linked to the Human Leukocyte Antigen Complex Includes at Least One Non–Class II Gene Lie, Benedicte A.
1999
64 3 p. 793-800
8 p.
artikel
34 The Transmission/Disequilibrium Test and Parental-Genotype Reconstruction: The Reconstruction-Combined Transmission/ Disequilibrium Test Knapp, Michael
1999
64 3 p. 861-870
10 p.
artikel
35 This Month in the Journal Ashkenas, John
1999
64 3 p. i-ii
nvt p.
artikel
                             35 gevonden resultaten
 
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