Volume 126, Issue 4

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October 2009

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12 articles in this issue

Analytical methods for inferring functional effects of single base pair substitutions in human cancers
William Lee
Peng Yue
Zemin Zhang
Review Article Open access 12 May 2009 Pages: 481 - 498
Genetic risk factors for melanoma
Kathrine Damm Meyle
Per Guldberg
Review Article 08 July 2009 Pages: 499 - 510
Different molecular mechanisms causing 9p21 deletions in acute lymphoblastic leukemia of childhood
Francesca Novara
Silvana Beri
Orsetta Zuffardi
Original Investigation Open access 30 May 2009 Pages: 511 - 520
Linguistic and maternal genetic diversity are not correlated in Native Mexicans
Karla Sandoval
Leonor Buentello-Malo
David Comas
Original Investigation Open access 04 June 2009 Pages: 521 - 531
In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation
Kandai Nozu
Kazumoto Iijima
Masafumi Matsuo
Original Investigation 10 June 2009 Pages: 533 - 538
Megakaryoblastic leukemia factor-1 gene in the susceptibility to coronary artery disease
Kunihiko Hinohara
Toshiaki Nakajima
Akinori Kimura
Original Investigation 10 June 2009 Pages: 539 - 547
Linkage of atopic dermatitis to chromosomes 4q22, 3p24 and 3q21
Ulla Christensen
Steffen Møller-Larsen
Anders D. Børglum
Original Investigation 11 June 2009 Pages: 549 - 557
Accelerated decline in lung function in cigarette smokers is associated with TP53/MDM2 polymorphisms
Robert J. Hancox
Richie Poulton
Antony W. Braithwaite
Original Investigation 12 June 2009 Pages: 559 - 565
Glucokinase regulatory protein gene polymorphism affects postprandial lipemic response in a dietary intervention study
Haiqing Shen
Toni I. Pollin
Alan R. Shuldiner
Original Investigation 13 June 2009 Pages: 567 - 574
A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1
Mounira Hmani-Aifa
Salma Ben Salem
Hammadi Ayadi
Original Investigation 14 June 2009 Pages: 575 - 587
Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping
Ayman W. El-Hattab
Teresa A. Smolarek
Pawel Stankiewicz
Original Investigation 26 June 2009 Pages: 589 - 602
Shaffer LG, Slovak ML, Campbell LJ (2009): ISCN 2009 an international system for human cytogenetic nomenclature
Lionel Willatt
Sian M. Morgan
Book Review 04 August 2009 Pages: 603 - 604

Volume 126, Issue 4

Analytical methods for inferring functional effects of single base pair substitutions in human cancers

Genetic risk factors for melanoma

Different molecular mechanisms causing 9p21 deletions in acute lymphoblastic leukemia of childhood

Linguistic and maternal genetic diversity are not correlated in Native Mexicans

In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation

Megakaryoblastic leukemia factor-1 gene in the susceptibility to coronary artery disease

Linkage of atopic dermatitis to chromosomes 4q22, 3p24 and 3q21

Accelerated decline in lung function in cigarette smokers is associated with TP53/MDM2 polymorphisms

Glucokinase regulatory protein gene polymorphism affects postprandial lipemic response in a dietary intervention study

A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1

Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping

Shaffer LG, Slovak ML, Campbell LJ (2009): ISCN 2009 an international system for human cytogenetic nomenclature

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