Lista de obras - Jean-Hubert Caberg - Dominio Público Uruguay

Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies

artículo científico publicado en 2014

Cytogenetic Studies of Rwandan Pediatric Patients Presenting with Global Developmental Delay, Intellectual Disability and/or Multiple Congenital Anomalies

artículo científico publicado en 2015

Exome copy number variation detection: Use of a pool of unrelated healthy tissue as reference sample

artículo científico publicado en 2016

Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation

artículo científico publicado en 2014

Haematological and molecular responses in refractory anaemia with ring sideroblasts and thrombocytosis treated with lenalidomide

artículo científico publicado en 2013

Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges

artículo científico

Increased migration of Langerhans cells in response to HPV16 E6 and E7 oncogene silencing: role of CCL20.

artículo científico publicado en 2008

MIP3 alpha stimulates the migration of Langerhans cells in models of human papillomavirus (HPV)-associated (pre)neoplastic epithelium

artículo científico publicado en 2006

Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy

artículo científico publicado en 2015

Partial trisomy 4q associated with young-onset dopa-responsive parkinsonism

artículo científico publicado en 2012

Pattern of congenital heart diseases in Rwandan children with genetic defects

artículo científico publicado en 2014

Role of hormone cofactors in the human papillomavirus-induced carcinogenesis of the uterine cervix

artículo científico publicado en 2006

Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1.

artículo científico publicado en 2014

Somatic mosaicism underlies X-linked acrogigantism syndrome in sporadic male subjects

artículo científico publicado en 2016

Surface Mucin-1 does not play a role in dendritic cell migration

artículo científico publicado en 2008

The cross-talk between dendritic and regulatory T cells: good or evil?

artículo científico publicado en 2007

X-linked acrogigantism syndrome: clinical profile and therapeutic responses

artículo científico publicado en 2015

Lista de obras de Jean-Hubert Caberg

Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies

Cytogenetic Studies of Rwandan Pediatric Patients Presenting with Global Developmental Delay, Intellectual Disability and/or Multiple Congenital Anomalies

Exome copy number variation detection: Use of a pool of unrelated healthy tissue as reference sample

Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation

Haematological and molecular responses in refractory anaemia with ring sideroblasts and thrombocytosis treated with lenalidomide

Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges

Increased migration of Langerhans cells in response to HPV16 E6 and E7 oncogene silencing: role of CCL20.

MIP3 alpha stimulates the migration of Langerhans cells in models of human papillomavirus (HPV)-associated (pre)neoplastic epithelium

Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy

Partial trisomy 4q associated with young-onset dopa-responsive parkinsonism

Pattern of congenital heart diseases in Rwandan children with genetic defects

Role of hormone cofactors in the human papillomavirus-induced carcinogenesis of the uterine cervix

Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1.

Somatic mosaicism underlies X-linked acrogigantism syndrome in sporadic male subjects

Surface Mucin-1 does not play a role in dendritic cell migration

The cross-talk between dendritic and regulatory T cells: good or evil?

X-linked acrogigantism syndrome: clinical profile and therapeutic responses