author-photo

Kristin Bosse

University of Bonn

11

Papers

310

Citations

Citation Trend

Filter By

Papers (6) Sort By

Journal Conference Others

Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis

2011 American Journal of Human Genetics
Show All
- Source
- Cite
- Save
Citations (81)
Further Delineation of the Phenotype Maps for Partial Trisomy 16q24 and Jacobsen Syndrome by a Subtle Familial Translocation t(11;16)(q24.2;q24.1)

2005 American Journal of Medical Genetics Part A
Show All
- Source
- Cite
- Save
Citations (20)
Unbalanced translocation 8;Y (45,X,dic(Y;8)(q11.23;p23.1)): case report and review of terminal 8p deletions.

2004 Annales De Genetique
Show All
- Source
- Cite
- Save
Citations (7)
Primary Congenital Glaucoma: A Novel Single-Nucleotide Deletion and Varying Phenotypic Expression for the 1546–1555dup Mutation in the GLC3A (CYP1B1) Gene in 2 Families of Different Ethnic Origin

2003 Journal of Glaucoma
Show All
- Source
- Cite
- Save
Citations (31)
Comprehensive analysis of human subtelomeres with combined binary ratio labelling fluorescence in situ hybridisation

2003 European Journal of Human Genetics
Show All
- Source
- Cite
- Save
Citations (20)
Further case of Cantú syndrome: Exclusion of cryptic subtelomeric chromosome aberrations

2002 American Journal of Medical Genetics
Show All
- Source
- Cite
- Save
Citations (25)