Search research articles
Contact Us
Filters
Showing results (1-10 of 29) with videos related to
Page
of 3
Sort By:
American Journal of Medical Genetics
|
September 12, 2000
Genetic heterogeneity in Noonan syndrome: evidence for an autosomal recessive form
I van Der Burgt, H Brunner
Journal of Medical Genetics
|
February 1, 1996
Nijmegen breakage syndrome
I van der Burgt, K H Chrzanowska, D Smeets, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 13, 2004
Growth hormone treatment in cartilage-hair hypoplasia: effects on growth and the immune system
G Bocca, C M Weemaes, I van der Burgt, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 5, 2009
Impaired Sertoli cell function in males diagnosed with Noonan syndrome
K A Marcus, C G J Sweep, I van der Burgt, et al.
Clinical Dysmorphology
|
October 23, 2001
3-M syndrome: description of six new patients with review of the literature
G van der Wal, B J Otten, H G Brunner, et al.
American Journal of Medical Genetics
|
November 1, 1994
Clinical and molecular studies in a large Dutch family with Noonan syndrome
I van der Burgt, E Berends, E Lommen, et al.
Prenatal Diagnosis
|
May 10, 2002
Isolated sulfite oxidase deficiency: mutation analysis and DNA-based prenatal diagnosis
J L Johnson, K V Rajagopalan, W O Renier, et al.
American Journal of Medical Genetics
|
December 1, 1991
Cartilage hair hypoplasia, metaphyseal chondrodysplasia type McKusick: description of seven patients and review of the literature
I van der Burgt, A Haraldsson, J C Oosterwijk, et al.
Psychological Medicine
|
July 12, 2011
Affective functioning and social cognition in Noonan syndrome
E Wingbermühle, J I M Egger, W M A Verhoeven, et al.
Hormone Research
|
February 16, 2002
Effects of growth hormone treatment on left ventricular dimensions in children with Noonan's syndrome
C Noordam, J M Draaisma, J van den Nieuwenhof, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 29) with videos related to
Sort By:
Page
of 3
American Journal of Medical Genetics
|
September 12, 2000
Genetic heterogeneity in Noonan syndrome: evidence for an autosomal recessive form
I van Der Burgt, H Brunner
Journal of Medical Genetics
|
February 1, 1996
Nijmegen breakage syndrome
I van der Burgt, K H Chrzanowska, D Smeets, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 13, 2004
Growth hormone treatment in cartilage-hair hypoplasia: effects on growth and the immune system
G Bocca, C M Weemaes, I van der Burgt, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 5, 2009
Impaired Sertoli cell function in males diagnosed with Noonan syndrome
K A Marcus, C G J Sweep, I van der Burgt, et al.
Clinical Dysmorphology
|
October 23, 2001
3-M syndrome: description of six new patients with review of the literature
G van der Wal, B J Otten, H G Brunner, et al.
American Journal of Medical Genetics
|
November 1, 1994
Clinical and molecular studies in a large Dutch family with Noonan syndrome
I van der Burgt, E Berends, E Lommen, et al.
Prenatal Diagnosis
|
May 10, 2002
Isolated sulfite oxidase deficiency: mutation analysis and DNA-based prenatal diagnosis
J L Johnson, K V Rajagopalan, W O Renier, et al.
American Journal of Medical Genetics
|
December 1, 1991
Cartilage hair hypoplasia, metaphyseal chondrodysplasia type McKusick: description of seven patients and review of the literature
I van der Burgt, A Haraldsson, J C Oosterwijk, et al.
Psychological Medicine
|
July 12, 2011
Affective functioning and social cognition in Noonan syndrome
E Wingbermühle, J I M Egger, W M A Verhoeven, et al.
Hormone Research
|
February 16, 2002
Effects of growth hormone treatment on left ventricular dimensions in children with Noonan's syndrome
C Noordam, J M Draaisma, J van den Nieuwenhof, et al.
Page
of 3