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Experimental Brain Research
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June 21, 2005
Visual depth processing in Williams-Beuren syndrome
J N Van der Geest, G C Lagers-van Haselen, J M van Hagen, et al.
Genes, Brain, and Behavior
|
July 12, 2008
Savings and extinction of conditioned eyeblink responses in fragile X syndrome
A E Smit, J N van der Geest, M Vellema, et al.
Journal of Medical Genetics
|
August 6, 2002
Silver-Russell phenotype in a patient with pure trisomy 1q32.1-q42.1: further delineation of the pure 1q trisomy syndrome
M M van Haelst, H J F M M Eussen, F Visscher, et al.
Journal of Medical Genetics
|
December 4, 2009
Phenotype-genotype correlation in a familial IGF1R microdeletion case
D C M Veenma, H J Eussen, L C P Govaerts, et al.
Neuropsychologia
|
January 17, 2004
Saccade dysmetria in Williams-Beuren syndrome
J N van der Geest, G C Lagers-van Haselen, J M van Hagen, et al.
Human Reproduction (Oxford, England)
|
January 5, 2002
Genetic risk factors in infertile men with severe oligozoospermia and azoospermia
G R Dohle, D J J Halley, J O Van Hemel, et al.
Acta Gastro-Enterologica Belgica
|
December 1, 1973
[Endoscopic cholangio-wirsungography in the diagnosis of obstructive jaundice (author's transl)]
M Cremer, L Engelholm, A Gulbis, et al.
American Journal of Medical Genetics. Part A
|
March 21, 2013
Another rare prenatal case of post-zygotic mosaic trisomy 17
Femke A T de Vries, Lutgarde C P Govaerts, Jeroen Knijnenburg, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 30, 2009
Two short children born small for gestational age with insulin-like growth factor 1 receptor haploinsufficiency illustrate the heterogeneity of its phenotype
Wietske A Ester, Hermine A van Duyvenvoorde, Caroline C de Wit, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
May 29, 2010
Omphalocele: comparison of outcome following prenatal or postnatal diagnosis
T E Cohen-Overbeek, W H Tong, T R Hatzmann, et al.
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of 9
Search research articles
Search
Showing results (51-60 of 84) with videos related to
Sort By:
Page
of 9
Experimental Brain Research
|
June 21, 2005
Visual depth processing in Williams-Beuren syndrome
J N Van der Geest, G C Lagers-van Haselen, J M van Hagen, et al.
Genes, Brain, and Behavior
|
July 12, 2008
Savings and extinction of conditioned eyeblink responses in fragile X syndrome
A E Smit, J N van der Geest, M Vellema, et al.
Journal of Medical Genetics
|
August 6, 2002
Silver-Russell phenotype in a patient with pure trisomy 1q32.1-q42.1: further delineation of the pure 1q trisomy syndrome
M M van Haelst, H J F M M Eussen, F Visscher, et al.
Journal of Medical Genetics
|
December 4, 2009
Phenotype-genotype correlation in a familial IGF1R microdeletion case
D C M Veenma, H J Eussen, L C P Govaerts, et al.
Neuropsychologia
|
January 17, 2004
Saccade dysmetria in Williams-Beuren syndrome
J N van der Geest, G C Lagers-van Haselen, J M van Hagen, et al.
Human Reproduction (Oxford, England)
|
January 5, 2002
Genetic risk factors in infertile men with severe oligozoospermia and azoospermia
G R Dohle, D J J Halley, J O Van Hemel, et al.
Acta Gastro-Enterologica Belgica
|
December 1, 1973
[Endoscopic cholangio-wirsungography in the diagnosis of obstructive jaundice (author's transl)]
M Cremer, L Engelholm, A Gulbis, et al.
American Journal of Medical Genetics. Part A
|
March 21, 2013
Another rare prenatal case of post-zygotic mosaic trisomy 17
Femke A T de Vries, Lutgarde C P Govaerts, Jeroen Knijnenburg, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 30, 2009
Two short children born small for gestational age with insulin-like growth factor 1 receptor haploinsufficiency illustrate the heterogeneity of its phenotype
Wietske A Ester, Hermine A van Duyvenvoorde, Caroline C de Wit, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
May 29, 2010
Omphalocele: comparison of outcome following prenatal or postnatal diagnosis
T E Cohen-Overbeek, W H Tong, T R Hatzmann, et al.
Page
of 9