Publikationen von Stefan Mundlos
Alle Typen
Zeitschriftenartikel (250)
241.
Zeitschriftenartikel
161 (11), S. 619 - 622 (2002)
Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasia. European Journal of Pediatrics 242.
Zeitschriftenartikel
161 (11), S. 623 - 626 (2002)
Severe cleidocranial dysplasia can mimic hypophosphatasia. European Journal of Pediatrics 243.
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 244.
Zeitschriftenartikel
245 (1), S. 95 - 108 (2002)
Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 245.
Zeitschriftenartikel
245 (1), S. 95 - 108 (2002)
Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 246.
Zeitschriftenartikel
245 (1), S. 95 - 108 (2002)
Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 247.
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 248.
Zeitschriftenartikel
19 (3), S. 209 - 216 (2002)
Mutations in the RUNX2 gene in patients with cleidocranial dysplasia. Human Mutation 249.
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 250.
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)
251.
Buch
Limb Malformations – An Atlas of Genetic Disorders of Limb Development. Springer-Verlag, Berlin, Heidelberg (2014), 767 S.
Konferenzbeitrag (1)
252.
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)
253.
Sonstige
Functional dissection of TADs reveals non-essential and instructive roles in regulating gene expression, bioRxiv (Preprint Server) 2019, (2019)
Manuskript (1)
254.
Manuskript
Genetic Diagnostics in Routine Osteological Assessment of Adult Low Bone Mass Disorders. Journal of Clinical Endocrinology and Metabolism, dgac147 (2022)
Review Article (1)
255.
Review Article
3D or Not 3D: Shaping the Genome during Development. (2021)
Preprint (2)
256.
Preprint
Combinatorial effects on gene expression at the Lbx1/Fgf8 locus resolve Split-Hand/Foot Malformation type 3. (2022)
257.
Preprint
Promoter repression and 3D-restructuring resolves divergent developmental gene expression in TADs. (2021)