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Publications by T Erhart Kinst
Low-Penetrance of RB-1 Gene Mutation in Familial Retinoblastoma 135
Pediatric Research
Child Health
Pediatrics
Perinatology
Related publications
Molecular Basis of Low-Penetrance Retinoblastoma
Archives of Ophthalmology
Familial Mutation in Caffey Disease With Reduced Penetrance: A Case Report
Turkish Journal of Pediatrics
Child Health
Pediatrics
Perinatology
A T to C Mutation in the Polypyrimidine Tract of the Exon 9 Splicing Site of the RB1 Gene Responsible for Low Penetrance Hereditary Retinoblastoma
Journal of Medical Genetics
Genetics
Mutation Analysis of the MEN1 Gene in Multiple Endocrine Neoplasia Type 1, Familial Acromegaly and Familial Isolated Hyperparathyroidism
Journal of Clinical Endocrinology and Metabolism
Biochemistry
Endocrinology
Clinical Biochemistry
Medicine
Metabolism
Diabetes
Identification of a Novel Mevalonate Kinase Gene Mutation in Combination With the Common MVK V377I Substitution and the Low-Penetrance TNFRSF1A R92Q Mutation
European Journal of Human Genetics
Genetics
Generation of a Retinoblastoma (Rb)1-Inducible Dominant-Negative (DN) Mouse Model
Frontiers in Cellular Neuroscience
Molecular Neuroscience
Cellular
A Novel Mutation in the Connexin 46 Gene Causes Autosomal Dominant Congenital Cataract With Incomplete Penetrance
Journal of Medical Genetics
Genetics
Retinoblastoma (Rb) Protein Upregulates Expression of the Ifi202 Gene Encoding an Interferon-Inducible Negative Regulator of Cell Growth
Oncogene
Cancer Research
Genetics
Molecular Biology
Growth Suppression by an E2f-Binding-Defective Retinoblastoma Protein (RB): Contribution From the RB C Pocket
Molecular and Cellular Biology
Cell Biology
Molecular Biology
