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Klinische Padiatrie
|
November 9, 2010
Malignant melanoma and Wiedemann-Beckwith syndrome in childhood
E Livingstone, A Caliebe, F Egberts, et al.
Anaesthesia
|
February 14, 2012
A comparison of the Nexfin® and transcardiopulmonary thermodilution to estimate cardiac output during coronary artery surgery
O Broch, J Renner, M Gruenewald, et al.
Molecular Syndromology
|
April 19, 2012
Novel Tandem Duplication in Exon 1 of the SNURF/SNRPN Gene in a Child with Transient Excessive Eating Behaviour and Weight Gain
S Naik, N S Thomas, J H Davies, et al.
American Journal of Medical Genetics. Part A
|
April 2, 2004
Phenotypical variation in cousins with the identical partial trisomy 9 (pter-q22.2) and 7 (q35-qter) at 16 and 23 weeks gestation
S Metzke-Heidemann, H Kuhling-von Kaisenberg, A Caliebe, et al.
European Journal of Medical Genetics
|
November 9, 2011
Bladder exstrophy and extreme genital anomaly in a patient with pure terminal 1q deletion: expansion of phenotypic spectrum
M S Zaki, G Gillessen-Kaesbach, I Vater, et al.
Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin
|
August 9, 2012
[Pediatric fracture diagnosis--ultra-low-dose CT with an effective dose equal to that of radiographs]
J D Moritz, B Hoffmann, D H Sehr, et al.
Genes and Immunity
|
January 24, 2014
SPAG7 is a candidate gene for the periodic fever, aphthous stomatitis, pharyngitis and adenopathy (PFAPA) syndrome
S Bens, T Zichner, A M Stütz, et al.
Clinical Pharmacology and Therapeutics
|
December 29, 2006
CYP3A5 genotype markedly influences the pharmacokinetics of tacrolimus and sirolimus in kidney transplant recipients
L Renders, M Frisman, M Ufer, et al.
Anticancer Research
|
August 23, 2000
The recombinant human histones H1 zero and H1.2 cause different toxicity profiles on the human leukemia cell line K562
K Pohlmeyer, J Broer, G Mayer, et al.
The British Journal of Dermatology
|
June 3, 1999
The wide spectrum of clinical expression in Adams-Oliver syndrome: a report of two cases
M Mempel, D Abeck, I Lange, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 30) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 30 results.
Klinische Padiatrie
|
November 9, 2010
Malignant melanoma and Wiedemann-Beckwith syndrome in childhood
E Livingstone, A Caliebe, F Egberts, et al.
Anaesthesia
|
February 14, 2012
A comparison of the Nexfin® and transcardiopulmonary thermodilution to estimate cardiac output during coronary artery surgery
O Broch, J Renner, M Gruenewald, et al.
Molecular Syndromology
|
April 19, 2012
Novel Tandem Duplication in Exon 1 of the SNURF/SNRPN Gene in a Child with Transient Excessive Eating Behaviour and Weight Gain
S Naik, N S Thomas, J H Davies, et al.
American Journal of Medical Genetics. Part A
|
April 2, 2004
Phenotypical variation in cousins with the identical partial trisomy 9 (pter-q22.2) and 7 (q35-qter) at 16 and 23 weeks gestation
S Metzke-Heidemann, H Kuhling-von Kaisenberg, A Caliebe, et al.
European Journal of Medical Genetics
|
November 9, 2011
Bladder exstrophy and extreme genital anomaly in a patient with pure terminal 1q deletion: expansion of phenotypic spectrum
M S Zaki, G Gillessen-Kaesbach, I Vater, et al.
Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin
|
August 9, 2012
[Pediatric fracture diagnosis--ultra-low-dose CT with an effective dose equal to that of radiographs]
J D Moritz, B Hoffmann, D H Sehr, et al.
Genes and Immunity
|
January 24, 2014
SPAG7 is a candidate gene for the periodic fever, aphthous stomatitis, pharyngitis and adenopathy (PFAPA) syndrome
S Bens, T Zichner, A M Stütz, et al.
Clinical Pharmacology and Therapeutics
|
December 29, 2006
CYP3A5 genotype markedly influences the pharmacokinetics of tacrolimus and sirolimus in kidney transplant recipients
L Renders, M Frisman, M Ufer, et al.
Anticancer Research
|
August 23, 2000
The recombinant human histones H1 zero and H1.2 cause different toxicity profiles on the human leukemia cell line K562
K Pohlmeyer, J Broer, G Mayer, et al.
The British Journal of Dermatology
|
June 3, 1999
The wide spectrum of clinical expression in Adams-Oliver syndrome: a report of two cases
M Mempel, D Abeck, I Lange, et al.
Page
of 3