Latest papers

Majewski osteodysplastic primordial dwarfism type II (MOPD II) syndrome previously diagnosed as Seckel syndrome: report of a novel mutation of the PCNT gene.

Spine Deformities in Rare Congenital Syndromes

A novel ENU-induced mutation, peewee, causes dwarfism in the mouse.

[Interview with Horst Stengritt (interview by Angelika Staub)].

Mice hypomorphic for Atr have increased DNA damage and abnormal checkpoint response.

Seckel syndrome and moyamoya.

Health-Related Quality of Life of Children and Adolescents with Growth Hormone Deficiency or Idiopathic Short Stature – Part 2: Available Results and Future Directions

Performance comparison of dwarf laying hens segregating for the naked neck gene in temperate and subtropical environments.

Morphometric analysis of the skull of the Sahel goat breed: basic and clinical anatomy.

Assessment of Health-Related Quality of Life and Patient Satisfaction in Children and Adolescents with Growth Hormone Deficiency or Idiopathic Short Stature – Part 1: A Critical Evaluation of Available Tools

Deletion of Xpter encompassing the SHOX gene and PAR1 region in familial patients with Leri-Weill Dyschondrosteosis syndrome.

Characterization of the dwg mutations: dwg and dwg(Bayer) are new mutant alleles of the Ggt1 gene.

Skeletal dysplasia in ancient Egypt.

The petit rat (pet/pet), a new semilethal mutant dwarf rat with thymic and testicular anomalies.

[Bone dysplasia with short limb].

[A case report of Silver-Russell syndrome].

Phenotypic characterization of the Komeda miniature rat Ishikawa, an animal model of dwarfism caused by a mutation in Prkg2.

Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic or Hall type: report of a case with normal face and literature review.

Overexpression of bone sialoprotein leads to an uncoupling of bone formation and bone resorption in mice.

Endothelial function and vascular oxidative stress in long-lived GH/IGF-deficient Ames dwarf mice.