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B C J Hamel

Showing results (1-10 of 23) with videos related to

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Clinical Genetics|April 29, 2005
X-linked mental retardation: further lumping, splitting and emerging phenotypesT Kleefstra, B C J Hamel
Genetic Counseling (Geneva, Switzerland)|August 2, 2002
Unexpected findings in identifiable stored blood samples after analysis without consent: moral arguments for and against disclosureM F Verweij, B C J Hamel
Journal of Medical Genetics|June 19, 2002
The p63 gene in EEC and other syndromesH G Brunner, B C J Hamel, H Van Bokhoven
Journal of Neurology|February 18, 2009
Joint hypermobility as a distinctive feature in the differential diagnosis of myopathiesN C Voermans, C G Bonnemann, B C J Hamel, et al.
International Journal of Hematology|June 8, 2011
Need for early recognition and therapeutic guidelines of congenital sideroblastic anaemiaM L H Cuijpers, D J van Spronsen, P Muus, et al.
Clinical Dysmorphology|February 6, 2002
Intestinal mucosa on top of a rudimentary occipital meningocele in amniotic rupture sequence: disorganization-like syndrome, homeotic transformation, abnormal surface encounter or endoectodermal adhesion?H J ten Donkelaar, B C J Hamel, E Hartman, et al.
European Journal of Pediatrics|May 12, 2009
Jeune syndrome: description of 13 cases and a proposal for follow-up protocolJ de Vries, J L Yntema, C E van Die, et al.
Molecular Syndromology|June 7, 2012
Adult Phenotypes in Angelman- and Rett-Like SyndromesM H Willemsen, J H M Rensen, H M J van Schrojenstein-Lantman de Valk, et al.
Clinical Genetics|August 16, 2003
No justification of routine screening for 22q11 deletions in patients with overt cleft palateE M Ruiter, E M H F Bongers, D F C M Smeets, et al.
Genetic Counseling (Geneva, Switzerland)|April 28, 2010
A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case reportF E P Mundhofir, A J A Kooper, T I Winarni, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Clinical Genetics|April 29, 2005
X-linked mental retardation: further lumping, splitting and emerging phenotypesT Kleefstra, B C J Hamel
Genetic Counseling (Geneva, Switzerland)|August 2, 2002
Unexpected findings in identifiable stored blood samples after analysis without consent: moral arguments for and against disclosureM F Verweij, B C J Hamel
Journal of Medical Genetics|June 19, 2002
The p63 gene in EEC and other syndromesH G Brunner, B C J Hamel, H Van Bokhoven
Journal of Neurology|February 18, 2009
Joint hypermobility as a distinctive feature in the differential diagnosis of myopathiesN C Voermans, C G Bonnemann, B C J Hamel, et al.
International Journal of Hematology|June 8, 2011
Need for early recognition and therapeutic guidelines of congenital sideroblastic anaemiaM L H Cuijpers, D J van Spronsen, P Muus, et al.
Clinical Dysmorphology|February 6, 2002
Intestinal mucosa on top of a rudimentary occipital meningocele in amniotic rupture sequence: disorganization-like syndrome, homeotic transformation, abnormal surface encounter or endoectodermal adhesion?H J ten Donkelaar, B C J Hamel, E Hartman, et al.
European Journal of Pediatrics|May 12, 2009
Jeune syndrome: description of 13 cases and a proposal for follow-up protocolJ de Vries, J L Yntema, C E van Die, et al.
Molecular Syndromology|June 7, 2012
Adult Phenotypes in Angelman- and Rett-Like SyndromesM H Willemsen, J H M Rensen, H M J van Schrojenstein-Lantman de Valk, et al.
Clinical Genetics|August 16, 2003
No justification of routine screening for 22q11 deletions in patients with overt cleft palateE M Ruiter, E M H F Bongers, D F C M Smeets, et al.
Genetic Counseling (Geneva, Switzerland)|April 28, 2010
A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case reportF E P Mundhofir, A J A Kooper, T I Winarni, et al.
Pageof 3