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4. Effect of mutation type and location on clinical outcome in 1,013 probands with marfan syndrome or related phenotypes and FBN1 mutations: an international study

6. The new Ghent criteria for Marfan syndrome: what do they change?

7. Pathogenic FBN1 Mutations in 146 Adults Not Meeting Clinical Diagnostic Criteria for Marfan Syndrome: Further Delineation of Type 1 Fibrillinopathies and Focus on Patients With an Isolated Major Criterion

11. Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands

18. A regular pattern of two types of 100-residue motif in the sequence of titin

40. CD14 is a member of the family of leucine-rich proteins and is encoded by a gene syntenic with multiple receptor genes

43. Cloning, sequencing, and expression of the gene coding for the human platelet alpha-2-adrenergic receptor

44. The gene for replication factor C subunit 2 (RFC2) is within the 7q11.23 Williams syndrome deletion

45. Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth

46. Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome

47. Cloning and regional assignment of the human myosin heavy chain 12 (MYH12) gene to chromosome band 15q21

48. The new Ghent criteria for Marfan syndrome: what do they change?

49. Gene for the alpha-subunit of the human interleukin-3 receptor (IL3RA) localized to the X-Y pseudoautosomal region

50. Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24–32 mutation

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