Volume 122, Issue 6

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January 2008

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12 articles in this issue

Discovering DNA: Friedrich Miescher and the early years of nucleic acid research
Ralf Dahm
Review Article 28 September 2007 Pages: 565 - 581
CFTR mutations and reproductive outcomes in a population isolate
Irene Gallego Romero
Carole Ober
Original Investigation 28 September 2007 Pages: 583 - 588
Localization of a novel gene for congenital nonsyndromic simple microphthalmia to chromosome 2q11-14
Hui Li
Jia-Xin Wang
Ya-Ping Zhang
Original Investigation 09 October 2007 Pages: 589 - 593
A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p
Marja W. Wessels
Bianca M. De Graaf
Patrick J. Willems
Original Investigation 16 October 2007 Pages: 595 - 603
Evidence for linkage of a new region (11p14) to eczema and allergic diseases
Michel Guilloud-Bataille
Emmanuelle Bouzigon
Marie-Hélène Dizier
Original Investigation 18 October 2007 Pages: 605 - 614
Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy
Minghui Qin
Hiroyuki Kondo
Kenshi Hayashi
Original Investigation 23 October 2007 Pages: 615 - 623
A genome-wide approach to identifying novel-imprinted genes
Katherine S. Pollard
David Serre
Kelly Frazer
Original Investigation 23 October 2007 Pages: 625 - 634
Induction of full-length survival motor neuron by polyphenol botanical compounds
Mary S. Sakla
Christian L. Lorson
Original Investigation 26 October 2007 Pages: 635 - 643
Functional characterization of the human TPH2 5′ regulatory region: untranslated region and polymorphisms modulate gene expression in vitro
Guo-Lin Chen
Eric J. Vallender
Gregory M. Miller
Original Investigation 31 October 2007 Pages: 645 - 657
Positive association between OLIG2 and schizophrenia in the Chinese Han population
Ke Huang
Wei Tang
YongYong Shi
Short Report 13 October 2007 Pages: 659 - 660
Parental transmission of HLA-DRB1*15 in multiple sclerosis
Sreeram V. Ramagopalan
Blanca M. Herrera
George C. Ebers
Short Report 31 October 2007 Pages: 661 - 663
Eberhard Passarge: Color atlas of genetics
Nicholas Robert Dennis
Book Review 19 October 2007 Pages: 665 - 665

Volume 122, Issue 6

Discovering DNA: Friedrich Miescher and the early years of nucleic acid research

CFTR mutations and reproductive outcomes in a population isolate

Localization of a novel gene for congenital nonsyndromic simple microphthalmia to chromosome 2q11-14

A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p

Evidence for linkage of a new region (11p14) to eczema and allergic diseases

Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy

A genome-wide approach to identifying novel-imprinted genes

Induction of full-length survival motor neuron by polyphenol botanical compounds

Functional characterization of the human TPH2 5′ regulatory region: untranslated region and polymorphisms modulate gene expression in vitro

Positive association between OLIG2 and schizophrenia in the Chinese Han population

Parental transmission of HLA-DRB115* in multiple sclerosis

Eberhard Passarge: Color atlas of genetics

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