Peters plus syndrome

[1]  J. Hoffman,et al.  Mutation analysis of B3GALTL in Peters Plus syndrome , 2008, American journal of medical genetics. Part A.

[2]  R. Hennekam,et al.  Peters Plus Syndrome Is a New Congenital Disorder of Glycosylation and Involves Defective O-Glycosylation of Thrombospondin Type 1 Repeats* , 2008, Journal of Biological Chemistry.

[3]  R. Hennekam,et al.  Peters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferase. , 2006, American journal of human genetics.

[4]  V. Kimonis,et al.  Peters Anomaly in Association with Multiple Midline Anomalies and a Familial Chromosome 4 Inversion , 2006, Ophthalmic genetics.

[5]  R. Hennekam,et al.  The Peters' plus syndrome: a review. , 2002, Annales de genetique.

[6]  I. Temple,et al.  Anterior chamber eye anomalies, redundant skin and syndactyly--a new syndrome associated with breakpoints at 2q37.2 and 7q36.3. , 1999, Clinical dysmorphology.

[7]  U. Mayer,et al.  Peters' anomaly and combination with other malformations (series of 16 patients). , 1992, Ophthalmic paediatrics and genetics.

[8]  G. Cibis,et al.  Peters' anomaly in association with ring 21 chromosomal abnormality. , 1985, American journal of ophthalmology.

[9]  C. Krantz.  Glycosylation of thrombospondin type 1 repeats , 2008 .

[10]  J. Bateman,et al.  Peters' anomaly associated with partial deletion of the long arm of chromosome 11. , 1984, American journal of ophthalmology.

[11]  F. Beemer,et al.  Peters'-plus: a new syndrome. , 1984, Ophthalmic paediatrics and genetics.