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Lancet (London, England)
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August 31, 1996
Search for genes predisposing to atopic diseases
H Scheffer
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde
|
January 1, 1973
Proceedings: Choroid melanoblastoma with signs of regression?
C H Scheffer, P G Binkhorst
American Journal of Medical Genetics. Part A
|
April 23, 2004
Ectodermal dysplasia with tetramelic deficiencies and no mutation in p63: odontotrichomelic syndrome or a new entity?
Andreas Zankl, H Scheffer, Albert Schinzel
Nederlands Tijdschrift Voor Geneeskunde
|
February 24, 2001
[Quality control of DNA testing in hereditary diseases]
A M van den Ouweland, H Scheffer
Nederlands Tijdschrift Voor Geneeskunde
|
January 17, 2002
[From gene to disease; 'survival' motor neuron protein and hereditary proximal spinal muscle atrophy]
J M Cobben, M de Visser, H Scheffer
Nederlands Tijdschrift Voor Geneeskunde
|
July 18, 2001
[From gene to disease; retinoblastoma and the RB1 gene]
H Scheffer, S M Imhof, A C Moll
Human Mutation
|
January 1, 1994
A novel mutation (G1249R) in exon 20 of the CFTR gene
D J Dijkstra, H Scheffer, C H Buys
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde
|
January 1, 1974
Malignant melanoma of the choroid in a 2-year-old infant
C H Scheffer, P G Binkhorst, A Hamburg
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association
|
June 5, 2007
Recurrent left-sided colon volvulus leading to mediastinal shift
Robert C H Scheffer, René J Wiezer, Robin Timmer
European Journal of Human Genetics : EJHG
|
July 21, 2001
Best practice guidelines for molecular analysis in spinal muscular atrophy
H Scheffer, J M Cobben, G Matthijs, et al.
Page
of 16
Search research articles
Search
Showing results (1-10 of 154) with videos related to
Sort By:
Page
of 16
Lancet (London, England)
|
August 31, 1996
Search for genes predisposing to atopic diseases
H Scheffer
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde
|
January 1, 1973
Proceedings: Choroid melanoblastoma with signs of regression?
C H Scheffer, P G Binkhorst
American Journal of Medical Genetics. Part A
|
April 23, 2004
Ectodermal dysplasia with tetramelic deficiencies and no mutation in p63: odontotrichomelic syndrome or a new entity?
Andreas Zankl, H Scheffer, Albert Schinzel
Nederlands Tijdschrift Voor Geneeskunde
|
February 24, 2001
[Quality control of DNA testing in hereditary diseases]
A M van den Ouweland, H Scheffer
Nederlands Tijdschrift Voor Geneeskunde
|
January 17, 2002
[From gene to disease; 'survival' motor neuron protein and hereditary proximal spinal muscle atrophy]
J M Cobben, M de Visser, H Scheffer
Nederlands Tijdschrift Voor Geneeskunde
|
July 18, 2001
[From gene to disease; retinoblastoma and the RB1 gene]
H Scheffer, S M Imhof, A C Moll
Human Mutation
|
January 1, 1994
A novel mutation (G1249R) in exon 20 of the CFTR gene
D J Dijkstra, H Scheffer, C H Buys
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde
|
January 1, 1974
Malignant melanoma of the choroid in a 2-year-old infant
C H Scheffer, P G Binkhorst, A Hamburg
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association
|
June 5, 2007
Recurrent left-sided colon volvulus leading to mediastinal shift
Robert C H Scheffer, René J Wiezer, Robin Timmer
European Journal of Human Genetics : EJHG
|
July 21, 2001
Best practice guidelines for molecular analysis in spinal muscular atrophy
H Scheffer, J M Cobben, G Matthijs, et al.
Page
of 16