| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Deleterious Mutation in SAMD9 Causes Normophosphatemic Familial Tumoral Calcinosis
|
Topaz, Orit
|
|
2006
|
79 |
4 |
p. 759-764
6 p.
|
artikel
|
| 2 |
A Flexible Bayesian Framework for Modeling Haplotype Association with Disease, Allowing for Dominance Effects of the Underlying Causative Variants
|
Morris, Andrew P.
|
|
2006
|
79 |
4 |
p. 679-694
16 p.
|
artikel
|
| 3 |
A Genomewide Search Finds Major Susceptibility Loci for Nicotine Dependence on Chromosome 10 in African Americans
|
Li, Ming D.
|
|
2006
|
79 |
4 |
p. 745-751
7 p.
|
artikel
|
| 4 |
A Genomewide Single-Nucleotide–Polymorphism Panel with High Ancestry Information for African American Admixture Mapping
|
Tian, Chao
|
|
2006
|
79 |
4 |
p. 640-649
10 p.
|
artikel
|
| 5 |
A New Method for Detecting Human Recombination Hotspots and Its Applications to the HapMap ENCODE Data
|
Li, Jun
|
|
2006
|
79 |
4 |
p. 628-639
12 p.
|
artikel
|
| 6 |
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.
|
|
|
2006
|
79 |
4 |
p. 774-777
4 p.
|
artikel
|
| 7 |
ASHG Takes Steps to Impact Undergraduate Genetics Education
|
Mills Shaw, Kenna R.
|
|
2006
|
79 |
4 |
p. 773-
1 p.
|
artikel
|
| 8 |
Colorectal Cancer Risk in Monoallelic Carriers of MYH Variants
|
Webb, Emily L.
|
|
2006
|
79 |
4 |
p. 768-771
4 p.
|
artikel
|
| 9 |
CRYBA4, a Novel Human Cataract Gene, Is Also Involved in Microphthalmia
|
Billingsley, Gail
|
|
2006
|
79 |
4 |
p. 702-709
8 p.
|
artikel
|
| 10 |
Familial Chilblain Lupus, a Monogenic Form of Cutaneous Lupus Erythematosus, Maps to Chromosome 3p
|
Lee-Kirsch, Min Ae
|
|
2006
|
79 |
4 |
p. 731-737
7 p.
|
artikel
|
| 11 |
Genetic Mapping at 3-Kilobase Resolution Reveals Inositol 1,4,5-Triphosphate Receptor 3 as a Risk Factor for Type 1 Diabetes in Sweden
|
Roach, Jared C.
|
|
2006
|
79 |
4 |
p. 614-627
14 p.
|
artikel
|
| 12 |
Genomewide Linkage Screen for Waldenström Macroglobulinemia Susceptibility Loci in High-Risk Families
|
McMaster, Mary L.
|
|
2006
|
79 |
4 |
p. 695-701
7 p.
|
artikel
|
| 13 |
HLA-B Maternal-Fetal Genotype Matching Increases Risk of Schizophrenia
|
Palmer, Christina G.S.
|
|
2006
|
79 |
4 |
p. 710-715
6 p.
|
artikel
|
| 14 |
Identification of the Gene Encoding the Enzyme Deficient in Mucopolysaccharidosis IIIC (Sanfilippo Disease Type C)
|
Fan, Xiaolian
|
|
2006
|
79 |
4 |
p. 738-744
7 p.
|
artikel
|
| 15 |
Linkage Analysis Identifies a Novel Locus for Restless Legs Syndrome on Chromosome 2q in a South Tyrolean Population Isolate
|
Pichler, Irene
|
|
2006
|
79 |
4 |
p. 716-723
8 p.
|
artikel
|
| 16 |
LRRK2 G2019S in Families with Parkinson Disease Who Originated from Europe and the Middle East: Evidence of Two Distinct Founding Events Beginning Two Millennia Ago
|
Zabetian, Cyrus P.
|
|
2006
|
79 |
4 |
p. 752-758
7 p.
|
artikel
|
| 17 |
Mutations in CABP4, the Gene Encoding the Ca2+-Binding Protein 4, Cause Autosomal Recessive Night Blindness
|
Zeitz, Christina
|
|
2006
|
79 |
4 |
p. 657-667
11 p.
|
artikel
|
| 18 |
Mutations in SLC34A2 Cause Pulmonary Alveolar Microlithiasis and Are Possibly Associated with Testicular Microlithiasis
|
Corut, Ayse
|
|
2006
|
79 |
4 |
p. 650-656
7 p.
|
artikel
|
| 19 |
Naegeli-Franceschetti-Jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations in KRT14
|
Lugassy, Jennie
|
|
2006
|
79 |
4 |
p. 724-730
7 p.
|
artikel
|
| 20 |
Origins of the Human Genome Project: Why Sequence the Human Genome When 96% of It Is Junk?
|
Berg, Paul
|
|
2006
|
79 |
4 |
p. 603-605
3 p.
|
artikel
|
| 21 |
Parent-of-Origin Effect and Risk for Attention-Deficit/Hyperactivity Disorder: Balancing the Evidence against Bias and Chance Findings
|
Joober, Ridha
|
|
2006
|
79 |
4 |
p. 765-766
2 p.
|
artikel
|
| 22 |
Reduction of Sample Heterogeneity through Use of Population Substructure: An Example from a Population of African American Families with Sarcoidosis
|
Thompson, Cheryl L.
|
|
2006
|
79 |
4 |
p. 606-613
8 p.
|
artikel
|
| 23 |
Reply to Joober and Sengupta
|
Segurado, Ricardo
|
|
2006
|
79 |
4 |
p. 766-768
3 p.
|
artikel
|
| 24 |
Reply to Webb et al.
|
Farrington, Susan M.
|
|
2006
|
79 |
4 |
p. 771-
1 p.
|
artikel
|
| 25 |
Satb2 Haploinsufficiency Phenocopies 2q32-q33 Deletions, whereas Loss Suggests a Fundamental Role in the Coordination of Jaw Development
|
Britanova, Olga
|
|
2006
|
79 |
4 |
p. 668-678
11 p.
|
artikel
|
| 26 |
This Month in the Journal
|
Williamson, Robin E.
|
|
2006
|
79 |
4 |
p. i-ii
nvt p.
|
artikel
|
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