| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal Dyspraxia
|
Feuk, Lars
|
|
2006
|
79 |
5 |
p. 965-972
8 p.
|
article
|
| 2 |
A Chromosomal Rearrangement Hotspot Can Be Identified from Population Genetic Variation and Is Coincident with a Hotspot for Allelic Recombination
|
Lindsay, Sarah J.
|
|
2006
|
79 |
5 |
p. 890-902
13 p.
|
article
|
| 3 |
Analysis of High-Resolution HapMap of DTNBP1 (Dysbindin) Suggests No Consistency between Reported Common Variant Associations and Schizophrenia
|
Mutsuddi, Mousumi
|
|
2006
|
79 |
5 |
p. 903-909
7 p.
|
article
|
| 4 |
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 ½-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 |
5 |
p. 987-990
4 p.
|
article
|
| 5 |
A Novel Mutation in FGFR3 Causes Camptodactyly, Tall Stature, and Hearing Loss (CATSHL) Syndrome
|
Toydemir, Reha M.
|
|
2006
|
79 |
5 |
p. 935-941
7 p.
|
article
|
| 6 |
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Associated with Mutations in the Desmosomal Gene Desmocollin-2
|
Syrris, Petros
|
|
2006
|
79 |
5 |
p. 978-984
7 p.
|
article
|
| 7 |
Detecting Disease-Causing Mutations in the Human Genome by Haplotype Matching
|
Spencer, David H.
|
|
2006
|
79 |
5 |
p. 958-964
7 p.
|
article
|
| 8 |
Distinct Clinical Phenotypes Associated with a Mutation in the Mitochondrial Translation Elongation Factor EFTs
|
Smeitink, Jan A.M.
|
|
2006
|
79 |
5 |
p. 869-877
9 p.
|
article
|
| 9 |
Epigenetic Allele Silencing Unveils Recessive RYR1 Mutations in Core Myopathies
|
Zhou, Haiyan
|
|
2006
|
79 |
5 |
p. 859-868
10 p.
|
article
|
| 10 |
Erratum
|
|
|
2006
|
79 |
5 |
p. 985-
1 p.
|
article
|
| 11 |
Generalized Genomic Distance–Based Regression Methodology for Multilocus Association Analysis
|
Wessel, Jennifer
|
|
2006
|
79 |
5 |
p. 792-806
15 p.
|
article
|
| 12 |
Mapping Trait Loci by Use of Inferred Ancestral Recombination Graphs
|
Minichiello, Mark J.
|
|
2006
|
79 |
5 |
p. 910-922
13 p.
|
article
|
| 13 |
Molecular Population Genetics of the Gene Encoding the Human Fertilization Protein Zonadhesin Reveals Rapid Adaptive Evolution
|
Gasper, Joe
|
|
2006
|
79 |
5 |
p. 820-830
11 p.
|
article
|
| 14 |
Multipoint Linkage Analysis with Many Multiallelic or Dense Diallelic Markers: Markov Chain–Monte Carlo Provides Practical Approaches for Genome Scans on General Pedigrees
|
Wijsman, Ellen M.
|
|
2006
|
79 |
5 |
p. 846-858
13 p.
|
article
|
| 15 |
Mutation in the Auxiliary Calcium-Channel Subunit CACNA2D4 Causes Autosomal Recessive Cone Dystrophy
|
Wycisk, Katharina Agnes
|
|
2006
|
79 |
5 |
p. 973-977
5 p.
|
article
|
| 16 |
Mutation-Positive and Mutation-Negative Patients with Cowden and Bannayan-Riley-Ruvalcaba Syndromes Associated with Distinct 10q Haplotypes
|
Pezzolesi, Marcus G.
|
|
2006
|
79 |
5 |
p. 923-934
12 p.
|
article
|
| 17 |
Mutations in the Tight-Junction Gene Claudin 19 (CLDN19) Are Associated with Renal Magnesium Wasting, Renal Failure, and Severe Ocular Involvement
|
Konrad, Martin
|
|
2006
|
79 |
5 |
p. 949-957
9 p.
|
article
|
| 18 |
Mutations in TMEM76 * Cause Mucopolysaccharidosis IIIC (Sanfilippo C Syndrome)
|
Hřebíček, Martin
|
|
2006
|
79 |
5 |
p. 807-819
13 p.
|
article
|
| 19 |
Mutations of the Mitochondrial Holocytochrome c–Type Synthase in X-Linked Dominant Microphthalmia with Linear Skin Defects Syndrome
|
Wimplinger, Isabella
|
|
2006
|
79 |
5 |
p. 878-889
12 p.
|
article
|
| 20 |
Nucleotide-Resolution Mapping of Topoisomerase-Mediated and Apoptotic DNA Strand Scissions at or near an MLL Translocation Hotspot
|
Mirault, Marc-Edouard
|
|
2006
|
79 |
5 |
p. 779-791
13 p.
|
article
|
| 21 |
PLA2G6 Mutation Underlies Infantile Neuroaxonal Dystrophy
|
Khateeb, Shareef
|
|
2006
|
79 |
5 |
p. 942-948
7 p.
|
article
|
| 22 |
Test for Interaction between Two Unlinked Loci
|
Zhao, Jinying
|
|
2006
|
79 |
5 |
p. 831-845
15 p.
|
article
|
| 23 |
This Month in the Journal
|
Williamson, Robin E.
|
|
2006
|
79 |
5 |
p. i-ii
nvt p.
|
article
|
| 24 |
What is FASEB, Anyway?
|
Boughman, Joann A.
|
|
2006
|
79 |
5 |
p. 986-
1 p.
|
article
|
Journal description