1. The molecular genetics of growth hormone deficiency

   • A. M. Procter
   • John A. Phillips III.
   • David N. Cooper

   Review 17 February 2014 Pages: 255 - 272

2. A functional polymorphism in the monoamine oxidase A gene promoter

   • S. Z. Sabol
   • Stella Hu
   • D. Hamer

   Rapid Communication 17 February 2014 Pages: 273 - 279

3. Variant in sulfonylurea receptor-1 gene is associated with high insulin concentrations in non-diabetic Mexican Americans: SUR-1 gene variant and hyperinsulinemia

   • Denise L. Goksel
   • Kathryn Fischbach
   • Peter O’Connell

   Rapid communication 17 February 2014 Pages: 280 - 285

4. A new L527R mutation of the βIGH3 gene in patients with lattice corneal dystrophy with deep stromal opacities

   • K. Fujiki
   • Yoshihiro Hotta
   • Atsushi Kanai

   Rapid Communication 17 February 2014 Pages: 286 - 289

5. Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome

   • Toshio Itoh
   • T. Tanaka
   • Yusuke Nakamura

   Original Investigation 17 February 2014 Pages: 290 - 294

6. The human FE65 gene: genomic structure and an intronic biallelic polymorphism associated with sporadic dementia of the Alzheimer type

   • Q. Hu
   • Walter A. Kukull
   • Samir S. Deeb

   Original Investigation 17 February 2014 Pages: 295 - 303

7. Identification of four novel mutations in the CYP21 gene in congenital adrenal hyperplasia in the Chinese

   • H.-H. Lee
   • Hsiang-Tai Chao
   • Bun-chu Chung

   Original Investigation 17 February 2014 Pages: 304 - 310

8. Molecular characterization of two deletion events involving Alu-sequences, one novel base substitution and two tentative hotspot mutations in the hypoxanthine phosphoribosyltransferase (HPRT) gene in five patients with Lesch-Nyhan syndrome

   • T. Tvrdik
   • Suzanne Marcus
   • Bo Lambert

   Original Investigation 17 February 2014 Pages: 311 - 318

9. Variability in the serotonin transporter gene and increased risk for major depression with melancholia

   • Blanca Gutiérrez
   • Luis Pintor
   • L. Fañanás

   Original Investigation 17 February 2014 Pages: 319 - 322

10. Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD)

    • Kazuhiro Kobayashi
    • Yutaka Nakahori
    • T. Toda

    Original Investigation 17 February 2014 Pages: 323 - 327

11. A novel locus for Leber congenital amaurosis on chromosome 14q24

    • David W. Stockton
    • Richard Alan Lewis
    • J. R. Lupski

    Original Investigation 17 February 2014 Pages: 328 - 333

12. New mechanism of BRCA-1 mutation by deletion/insertion at the same nucleotide position in three unrelated French breast/ovarian cancer families

    • Nadège Presneau
    • Valérie Laplace-Marieze
    • Y.-J. Bignon

    Original Investigation 17 February 2014 Pages: 334 - 339

13. The NIK protein kinase and C17orf1 genes: chromosomal mapping, gene structures and mutational screening in frontotemporal dementia and parkinsonism linked to chromosome 17

    • Fredrik C. Aronsson
    • Patrik Magnusson
    • A. J. Brookes

    Original Investigation 17 February 2014 Pages: 340 - 345

14. Genetic structure of five susceptibility gene regions for coronary artery disease: disequilibria within and among regions

    • K. E. Zerba
    • Robert E. Ferrell
    • Charles F. Sing

    Original Investigation 17 February 2014 Pages: 346 - 354

15. In silico-initiated cloning and molecular characterization of a novel human member of the L1 gene family of neural cell adhesion molecules

    • Ming-Hui Wei
    • Irina Karavanova
    • M. I. Lerman

    Original Investigation 17 February 2014 Pages: 355 - 364

16. Polymorphism in the FMR1 gene

    • Chris Gunter
    • S. T. Warren

    Letter to the editor 17 February 2014 Pages: 365 - 365

17. Regarding the letter from Dr. Stephen T. Warren of the Emory University School of Medicine concerning our article “Mutational analysis of the FMR1 gene in 118 mentally retarded males suspected of fragile X syndrome: absence of prevalent mutations”

    • Karen Grønskov
    • K. Brøndum-Nielsen

    Letter to the editor 17 February 2014 Pages: 366 - 366

18. Chromosomal instability in cancer patients

    • D. Toncheva
    • M. Nacheva

    Letter to the editor 17 February 2014 Pages: 367 - 369

19. Comments on the letter of Toncheva and Nacheva concerning our paper “Latent chromosomal instability in cancer patients”

    • D. Komitowski
    • M. Tzancheva

    Letter to the editor 17 February 2014 Pages: 370 - 371

20. ICRF handbook of genome analysis: Nigel K. Spurr, Bryan D. Young, Stephen P. Bryant (Editors)

    • Meena Upadhyaya

    Book Review 17 February 2014 Pages: 372 - 373

21. Gene symbol: NF2

    • C. Ehlers
    • R. Fahsold

    Human Gene Mutations 17 February 2014 Pages: 374 - 374