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International Journal of Pediatric Otorhinolaryngology
|
January 1, 1992
Hearing loss in Noonan syndrome
C W Cremers, C J van der Burgt
Clinical Dysmorphology
|
November 14, 1997
A female patient with neurological, facial, digital and renal abnormalities: another case of the neurofaciodigitorenal (NFDR) syndrome?
P Rump, M Y Gruijters, C J Van der Burgt
International Journal of Radiation Biology
|
December 1, 1994
Nijmegen Breakage syndrome: a progress report
C M Weemaes, D F Smeets, C J van der Burgt
American Journal of Medical Genetics
|
September 1, 1994
Familial Angelman syndrome with a crossover in the critical deletion region
M R Nelen, C J Van der Burgt, W N Nillesen, et al.
European Journal of Pediatrics
|
June 1, 1993
Antibody deficiency and isolated growth hormone deficiency in a girl with Mulibrey nanism
A Haraldsson, C J van der Burgt, C M Weemaes, et al.
Scandinavian Journal of Immunology
|
August 1, 1997
T cell subsets and T cell function in cartilage-hair hypoplasia
R Kooijman, C J van der Burgt, C M Weemaes, et al.
Clinical Dysmorphology
|
January 1, 1996
Ectrodactyly of lower limbs, congenital heart defect and characteristic facies in four unrelated Dutch patients: a new association
J J Van Den Ende, C J Van Der Burgt, M C Jansweijer, et al.
Journal of Medical Genetics
|
October 1, 1992
Partial trisomy for 5q and monosomy for 12p in a liveborn child as a result of a complex five breakpoint chromosome rearrangement in a parent
C J Van Der Burgt, G F Merkx, A H Janssen, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
February 3, 1990
[Human parvovirus B19 and pregnancy]
A M van Elsacker-Niele, C J van der Burgt, N G Hartwig, et al.
Acta Neuropathologica
|
December 1, 1996
Myopathology in patients with a Noonan phenotype
W P de Boode, B A Semmekrot, H J ter Laak, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
International Journal of Pediatric Otorhinolaryngology
|
January 1, 1992
Hearing loss in Noonan syndrome
C W Cremers, C J van der Burgt
Clinical Dysmorphology
|
November 14, 1997
A female patient with neurological, facial, digital and renal abnormalities: another case of the neurofaciodigitorenal (NFDR) syndrome?
P Rump, M Y Gruijters, C J Van der Burgt
International Journal of Radiation Biology
|
December 1, 1994
Nijmegen Breakage syndrome: a progress report
C M Weemaes, D F Smeets, C J van der Burgt
American Journal of Medical Genetics
|
September 1, 1994
Familial Angelman syndrome with a crossover in the critical deletion region
M R Nelen, C J Van der Burgt, W N Nillesen, et al.
European Journal of Pediatrics
|
June 1, 1993
Antibody deficiency and isolated growth hormone deficiency in a girl with Mulibrey nanism
A Haraldsson, C J van der Burgt, C M Weemaes, et al.
Scandinavian Journal of Immunology
|
August 1, 1997
T cell subsets and T cell function in cartilage-hair hypoplasia
R Kooijman, C J van der Burgt, C M Weemaes, et al.
Clinical Dysmorphology
|
January 1, 1996
Ectrodactyly of lower limbs, congenital heart defect and characteristic facies in four unrelated Dutch patients: a new association
J J Van Den Ende, C J Van Der Burgt, M C Jansweijer, et al.
Journal of Medical Genetics
|
October 1, 1992
Partial trisomy for 5q and monosomy for 12p in a liveborn child as a result of a complex five breakpoint chromosome rearrangement in a parent
C J Van Der Burgt, G F Merkx, A H Janssen, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
February 3, 1990
[Human parvovirus B19 and pregnancy]
A M van Elsacker-Niele, C J van der Burgt, N G Hartwig, et al.
Acta Neuropathologica
|
December 1, 1996
Myopathology in patients with a Noonan phenotype
W P de Boode, B A Semmekrot, H J ter Laak, et al.
Page
of 1