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Genetic Counseling (Geneva, Switzerland)
|
February 1, 2003
Hypertrichosis cubiti: two new cases and a review of the literature
R Visser, F A Beemer, R H Veenhoven, et al.
Clinical Genetics
|
January 1, 1985
Trisomy 10 mosaicism in a newborn boy; delineation of the syndrome
H F de France, F A Beemer, R C Senders, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
January 31, 2006
[Congenital myotonic dystrophy--the significance of a handshake]
J U M Termote, F A Beemer, D Wittebol-Post, et al.
American Journal of Medical Genetics
|
March 1, 1985
A new syndrome of dwarfism, neonatal death, narrow chest, spondylometaphyseal abnormalities, and advanced bone age
F A Beemer, P P Kramer, H J van der Harten, et al.
Surgery
|
July 1, 1997
Increased risk for inguinal hernia in patients with Ehlers-Danlos syndrome
M S Liem, Y van der Graaf, F A Beemer, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology
|
January 1, 1985
Neuropathological findings in a case of combined deficiency of sulphite oxidase and xanthine dehydrogenase
P G Barth, F A Beemer, B P Cats, et al.
American Journal of Diseases of Children (1960)
|
November 1, 1980
Molybdenum metabolism
F A Beemer, M Duran, S K Wadman, et al.
Clinical Biochemistry
|
December 1, 1979
Simultaneous occurrence of xanthine oxidase and sulfite oxidase deficiency. A molybdenum dependent inborn error of metabolism?
C van der Heiden, F A Beemer, W Brink, et al.
Ophthalmic Paediatrics and Genetics
|
December 1, 1984
Peters'-plus: a new syndrome
M J van Schooneveld, J W Delleman, F A Beemer, et al.
Nature Genetics
|
March 31, 2000
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
M J van den Boogaard, M Dorland, F A Beemer, et al.
Page
of 18
Search research articles
Search
Showing results (61-70 of 177) with videos related to
Sort By:
Page
of 18
Genetic Counseling (Geneva, Switzerland)
|
February 1, 2003
Hypertrichosis cubiti: two new cases and a review of the literature
R Visser, F A Beemer, R H Veenhoven, et al.
Clinical Genetics
|
January 1, 1985
Trisomy 10 mosaicism in a newborn boy; delineation of the syndrome
H F de France, F A Beemer, R C Senders, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
January 31, 2006
[Congenital myotonic dystrophy--the significance of a handshake]
J U M Termote, F A Beemer, D Wittebol-Post, et al.
American Journal of Medical Genetics
|
March 1, 1985
A new syndrome of dwarfism, neonatal death, narrow chest, spondylometaphyseal abnormalities, and advanced bone age
F A Beemer, P P Kramer, H J van der Harten, et al.
Surgery
|
July 1, 1997
Increased risk for inguinal hernia in patients with Ehlers-Danlos syndrome
M S Liem, Y van der Graaf, F A Beemer, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology
|
January 1, 1985
Neuropathological findings in a case of combined deficiency of sulphite oxidase and xanthine dehydrogenase
P G Barth, F A Beemer, B P Cats, et al.
American Journal of Diseases of Children (1960)
|
November 1, 1980
Molybdenum metabolism
F A Beemer, M Duran, S K Wadman, et al.
Clinical Biochemistry
|
December 1, 1979
Simultaneous occurrence of xanthine oxidase and sulfite oxidase deficiency. A molybdenum dependent inborn error of metabolism?
C van der Heiden, F A Beemer, W Brink, et al.
Ophthalmic Paediatrics and Genetics
|
December 1, 1984
Peters'-plus: a new syndrome
M J van Schooneveld, J W Delleman, F A Beemer, et al.
Nature Genetics
|
March 31, 2000
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
M J van den Boogaard, M Dorland, F A Beemer, et al.
Page
of 18