Publications of Stefan Mundlos
All genres
Journal Article (256)
241.
Journal Article
73 (3), pp. 447 - 474 (2003)
Genetic disorders of the skeleton: a developmental approach. American Journal of Human Genetics 242.
Journal Article
27 (8), pp. 673 - 684 (2003)
A single amphioxus and sea urchin runt-gene suggests that runt-gene duplications occurred in early chordate evolution. Developmental and Comparative Immunology 243.
Journal Article
8 (7), pp. 645 - 654 (2003)
The receptor tyrosine kinase Ror2 is involved in non-canonical Wnt5a/JNK signalling pathway. Genes to Cells 244.
Journal Article
278 (19), pp. 17360 - 17367 (2003)
Expression of galectin-3 in skeletal tissues is controlled by Runx2. Journal of Biological Chemistry 245.
Journal Article
278 (19), pp. 17360 - 17367 (2003)
Expression of galectin-3 in skeletal tissues is controlled by Runx2. Journal of Biological Chemistry 246.
Journal Article
120A (4), pp. 547 - 552 (2003)
Antenatal onset of cortical hyperostosis (Caffey disease): Case report and review. American Journal of Medical Genetics Part A 247.
Journal Article
161 (11), pp. 619 - 622 (2002)
Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasia. European Journal of Pediatrics 248.
Journal Article
161 (11), pp. 623 - 626 (2002)
Severe cleidocranial dysplasia can mimic hypophosphatasia. European Journal of Pediatrics 249.
Journal Article
51 (3), pp. 249 - 255 (2002)
Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy. Epilepsy Research 250.
Journal Article
245 (1), pp. 95 - 108 (2002)
Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 251.
Journal Article
245 (1), pp. 95 - 108 (2002)
Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 252.
Journal Article
245 (1), pp. 95 - 108 (2002)
Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 253.
Journal Article
22 (5), pp. 404 - 407 (2002)
Prenatal diagnosis of partial agenesis of the corpus callosum in a fetus with thanatophoric dysplasia type 2. Prenatal Diagnosis 254.
Journal Article
19 (3), pp. 209 - 216 (2002)
Mutations in the RUNX2 gene in patients with cleidocranial dysplasia. Human Mutation 255.
Journal Article
112 (1-2), pp. 53 - 67 (2002)
The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage eleme. Mechanisms of Development 256.
Journal Article
112 (1-2), pp. 53 - 67 (2002)
The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage eleme. Mechanisms of Development Book (1)
257.
Book
Limb Malformations – An Atlas of Genetic Disorders of Limb Development. Springer-Verlag, Berlin, Heidelberg (2014), 767 pp.
Conference Paper (1)
258.
Conference Paper
2015. Genome Regulation in 3D, Rehovot, Israel, June 28, 2015 - June 30, 2015. Weizmann Institute, Rehovot, Israel (2015)
Identification of potential regulatory elements in Capture-C interaction profiles. In: Genome Regulation in 3D, Vol. Other (1)
259.
Other
Functional dissection of TADs reveals non-essential and instructive roles in regulating gene expression, bioRxiv (Preprint Server) 2019, (2019)
Manuscript (1)
260.
Manuscript
Genetic Diagnostics in Routine Osteological Assessment of Adult Low Bone Mass Disorders. Journal of Clinical Endocrinology and Metabolism, dgac147 (2022)