C. Bosch

发表

Adenomatous polyposis coli-mediated control of β-catenin is essential for both chondrogenic and osteogenic differentia- tion of skeletal precursors

R. Fodde, T. Kobayashi, J. Wit, 2011 .

Adenomatous polyposis coli-mediated control of β-catenin is essential for both chondrogenic and osteogenic differentiation of skeletal precursors

R. Fodde, J. Wit, H. Kronenberg, 2009, BMC Developmental Biology.

IGF1, IGF1R and SHOX Mutation Analysis in Short Children Born Small for Gestational Age and Short Children with Normal Birth Size (Idiopathic Short Stature)

G. Binder, C. Ruivenkamp, M. Losekoot, 2012, Hormone Research in Paediatrics.

A 797 kb de novo deletion of 18q21.31 in a patient with speech delay, mental retardation, sleeping problems, facial dysmorphism, and feet anomalies.

C. Ruivenkamp, E. Bijlsma, A. Gijsbers, 2011, European journal of medical genetics.

Bmc Developmental Biology

R. Fodde, J. Wit, H. Kronenberg, 2022 .

Additional cryptic CNVs in mentally retarded patients with apparently balanced karyotypes.

Osdilly Giromus, E. Bakker, C. Ruivenkamp, 2010, European journal of medical genetics.

A new diagnostic workflow for patients with mental retardation and/or multiple congenital abnormalities: test arrays first

J. Schuurs-Hoeijmakers, A. Haeringen, E. Bakker, 2009, European Journal of Human Genetics.

Three new cases with a mosaicism involving a normal cell line and a cryptic unbalanced autosomal reciprocal translocation.

E. Bakker, C. Ruivenkamp, M. Breuning, 2011, European journal of medical genetics.

Mosaicism with a normal cell line and an unbalanced autosomal reciprocal translocation ; three new cases and review of the literature

Ende, E. Bakker, M. Breuning, 2010 .

A new conditional Apc-mutant mouse model for colorectal cancer.

P. Devilee, H. Verspaget, R. Fodde, 2010, Carcinogenesis.

Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement

Jacqueline K. White, R. Hennekam, J. T. Dunnen, 2012, Nature Genetics.

Familial Adenomatous Polyposis-Associated Desmoids Display Significantly More Genetic Changes than Sporadic Desmoids

B. Alman, P. Devilee, P. Radice, 2011, PloS one.

Copy Number Variants in Short Children Born Small for Gestational Age

J. Baron, J. Lui, G. Binder, 2014, Hormone Research in Paediatrics.

A Subtle Familial Translocation t(3;21)(p26.3;q22.3): An Apparently Healthy Boy with a 3p Deletion and 21q Duplication

A. Haeringen, E. Bakker, C. Ruivenkamp, 2010, Cytogenetic and Genome Research.

Chapter 4 . 2 A subtle familial translocation t ( 3 ; 21 ) ( p 26 . 3 ; q 22 . 3 ) : apparently healthy boy with a 3 p deletion and 21 q duplication

A. Haeringen, E. Bakker, K. Hansson, 2010 .

Adult‐onset beta‐thalassaemia intermedia caused by a 5‐Mb somatic clonal segmental deletion in haemopoietic stem cells involving the β‐globin locus

C. Ruivenkamp, E. Kanavakis, J. Traeger-Synodinos, 2019, British journal of haematology.

IGF1, IGF1R and SHOX Mutation Analysis in Short Children Born Small for Gestational Age and Short Children with Normal Birth Size (Idiopathic Short Stature)

G. Binder, C. Ruivenkamp, M. Losekoot, 2012, Hormone Research in Paediatrics.

A new conditional Apc-mutant mouse model for colorectal cancer.

P. Devilee, H. Verspaget, R. Fodde, 2010, Carcinogenesis.

Additional cryptic CNVs in mentally retarded patients with apparently balanced karyotypes.

Osdilly Giromus, E. Bakker, C. Ruivenkamp, 2010, European journal of medical genetics.