Publikationen von Stefan Mundlos
Alle Typen
Zeitschriftenartikel (256)
241.
Zeitschriftenartikel
73 (3), S. 447 - 474 (2003)
Genetic disorders of the skeleton: a developmental approach. American Journal of Human Genetics 242.
Zeitschriftenartikel
27 (8), S. 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.
Zeitschriftenartikel
8 (7), S. 645 - 654 (2003)
The receptor tyrosine kinase Ror2 is involved in non-canonical Wnt5a/JNK signalling pathway. Genes to Cells 244.
Zeitschriftenartikel
278 (19), S. 17360 - 17367 (2003)
Expression of galectin-3 in skeletal tissues is controlled by Runx2. Journal of Biological Chemistry 245.
Zeitschriftenartikel
278 (19), S. 17360 - 17367 (2003)
Expression of galectin-3 in skeletal tissues is controlled by Runx2. Journal of Biological Chemistry 246.
Zeitschriftenartikel
120A (4), S. 547 - 552 (2003)
Antenatal onset of cortical hyperostosis (Caffey disease): Case report and review. American Journal of Medical Genetics Part A 247.
Zeitschriftenartikel
161 (11), S. 619 - 622 (2002)
Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasia. European Journal of Pediatrics 248.
Zeitschriftenartikel
161 (11), S. 623 - 626 (2002)
Severe cleidocranial dysplasia can mimic hypophosphatasia. European Journal of Pediatrics 249.
Zeitschriftenartikel
51 (3), S. 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.
Zeitschriftenartikel
245 (1), S. 95 - 108 (2002)
Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 251.
Zeitschriftenartikel
245 (1), S. 95 - 108 (2002)
Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 252.
Zeitschriftenartikel
245 (1), S. 95 - 108 (2002)
Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 253.
Zeitschriftenartikel
22 (5), S. 404 - 407 (2002)
Prenatal diagnosis of partial agenesis of the corpus callosum in a fetus with thanatophoric dysplasia type 2. Prenatal Diagnosis 254.
Zeitschriftenartikel
19 (3), S. 209 - 216 (2002)
Mutations in the RUNX2 gene in patients with cleidocranial dysplasia. Human Mutation 255.
Zeitschriftenartikel
112 (1-2), S. 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.
Zeitschriftenartikel
112 (1-2), S. 53 - 67 (2002)
The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage eleme. Mechanisms of Development Buch (1)
257.
Buch
Limb Malformations – An Atlas of Genetic Disorders of Limb Development. Springer-Verlag, Berlin, Heidelberg (2014), 767 S.
Konferenzbeitrag (1)
258.
Konferenzbeitrag
2015. Genome Regulation in 3D, Rehovot, Israel, 28. Juni 2015 - 30. Juni 2015. Weizmann Institute, Rehovot, Israel (2015)
Identification of potential regulatory elements in Capture-C interaction profiles. In: Genome Regulation in 3D, Bd. Sonstige (1)
259.
Sonstige
Functional dissection of TADs reveals non-essential and instructive roles in regulating gene expression, bioRxiv (Preprint Server) 2019, (2019)
Manuskript (1)
260.
Manuskript
Genetic Diagnostics in Routine Osteological Assessment of Adult Low Bone Mass Disorders. Journal of Clinical Endocrinology and Metabolism, dgac147 (2022)