Search research articles
Contact Us
Filters
Showing results (1-10 of 23) with videos related to
Page
of 3
Sort By:
Clinical Genetics
|
April 29, 2005
X-linked mental retardation: further lumping, splitting and emerging phenotypes
T 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 disclosure
M F Verweij, B C J Hamel
Journal of Medical Genetics
|
June 19, 2002
The p63 gene in EEC and other syndromes
H 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 myopathies
N 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 anaemia
M 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 protocol
J de Vries, J L Yntema, C E van Die, et al.
Molecular Syndromology
|
June 7, 2012
Adult Phenotypes in Angelman- and Rett-Like Syndromes
M 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 palate
E 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 report
F E P Mundhofir, A J A Kooper, T I Winarni, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 23) with videos related to
Sort By:
Page
of 3
Clinical Genetics
|
April 29, 2005
X-linked mental retardation: further lumping, splitting and emerging phenotypes
T 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 disclosure
M F Verweij, B C J Hamel
Journal of Medical Genetics
|
June 19, 2002
The p63 gene in EEC and other syndromes
H 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 myopathies
N 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 anaemia
M 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 protocol
J de Vries, J L Yntema, C E van Die, et al.
Molecular Syndromology
|
June 7, 2012
Adult Phenotypes in Angelman- and Rett-Like Syndromes
M 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 palate
E 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 report
F E P Mundhofir, A J A Kooper, T I Winarni, et al.
Page
of 3