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Zeitschriftenartikel (239)
221.
Zeitschriftenartikel
124A (4), S. 356 - 363 (2004)
Brachydactyly type C caused by a homozygous missense mutation in the prodomain of CDMP1. American Journal of Medical Genetics 222.
Zeitschriftenartikel
11 (11), S. 858 - 865 (2003)
Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes. European Journal of Human Genetics 223.
Zeitschriftenartikel
100 (21), S. 12277 - 12282 (2003)
Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2. Proceedings of the National Academy of Sciences of the United States of America 224.
Zeitschriftenartikel
73 (3), S. 447 - 474 (2003)
Genetic disorders of the skeleton: a developmental approach. American Journal of Human Genetics 225.
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 226.
Zeitschriftenartikel
8 (7), S. 645 - 654 (2003)
The receptor tyrosine kinase Ror2 is involved in non-canonical Wnt5a/JNK signalling pathway. Genes to Cells 227.
Zeitschriftenartikel
278 (19), S. 17360 - 17367 (2003)
Expression of galectin-3 in skeletal tissues is controlled by Runx2. Journal of Biological Chemistry 228.
Zeitschriftenartikel
278 (19), S. 17360 - 17367 (2003)
Expression of galectin-3 in skeletal tissues is controlled by Runx2. Journal of Biological Chemistry 229.
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 230.
Zeitschriftenartikel
161 (11), S. 619 - 622 (2002)
Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasia. European Journal of Pediatrics 231.
Zeitschriftenartikel
161 (11), S. 623 - 626 (2002)
Severe cleidocranial dysplasia can mimic hypophosphatasia. European Journal of Pediatrics 232.
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 233.
Zeitschriftenartikel
245 (1), S. 95 - 108 (2002)
Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 234.
Zeitschriftenartikel
245 (1), S. 95 - 108 (2002)
Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 235.
Zeitschriftenartikel
245 (1), S. 95 - 108 (2002)
Role of Runx Genes in Chondrocyte Differentiation. Developmental Biology 236.
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 237.
Zeitschriftenartikel
19 (3), S. 209 - 216 (2002)
Mutations in the RUNX2 gene in patients with cleidocranial dysplasia. Human Mutation 238.
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 239.
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)
240.
Buch
Limb Malformations – An Atlas of Genetic Disorders of Limb Development. Springer-Verlag, Berlin, Heidelberg (2014), 767 S.