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Clinical Endocrinology
|
January 10, 2008
Facial and pituitary morphology are related in Dutch patients with GH deficiency
L C G de Graaff, J Baan, L C P Govaerts, et al.
The American Journal of Otology
|
December 10, 1997
Stimulation of epithelial healing in chronic postoperative otorrhea using lyophilized cultured keratinocyte lysates
T Somers, L Duinslaeger, B Delaey, et al.
Acta Oto-Rhino-Laryngologica Belgica
|
July 4, 1998
The LAURA Pediatric Cochlear Implant Program in Antwerp: what have we learnt in 5 years?
F E Offeciers, P Govaerts, K Daemers, et al.
American Journal of Medical Genetics. Part A
|
October 17, 2008
Phenotypic consequences of a novel SCO2 gene mutation
Rob M Verdijk, Ronald de Krijger, Kees Schoonderwoerd, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
January 31, 2019
[Incidental detection of maternal malignancy in non-invasive prenatal test]
Lotte Saes, Lutgarde C P Govaerts, Maarten F C M Knapen, et al.
European Journal of Human Genetics : EJHG
|
November 7, 2013
Types of array findings detectable in cytogenetic diagnosis: a proposal for a generic classification
Malgorzata I Srebniak, Karin E M Diderich, Lutgarde C P Govaerts, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
July 31, 2013
Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature
M C de Wit, M I Srebniak, L C P Govaerts, et al.
Clinical Genetics
|
July 31, 2007
Exceptional good cognitive and phenotypic profile in a male carrying a mosaic mutation in the FMR1 gene
L C P Govaerts, A E Smit, J J Saris, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 10, 2015
Is prenatal cytogenetic diagnosis with genomic array indicated in pregnancies at risk for a molecular or metabolic disorder?
Malgorzata I Srebniak, Lutgarde C P Govaerts, Karin E M Diderich, et al.
Prenatal Diagnosis
|
July 15, 2011
Outcome of pregnancies complicated by oligohydramnios or anhydramnios of renal origin
E W M Grijseels, P T M Echteld van-Hornstra, L C P Govaerts, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 84) with videos related to
Sort By:
Page
of 9
Clinical Endocrinology
|
January 10, 2008
Facial and pituitary morphology are related in Dutch patients with GH deficiency
L C G de Graaff, J Baan, L C P Govaerts, et al.
The American Journal of Otology
|
December 10, 1997
Stimulation of epithelial healing in chronic postoperative otorrhea using lyophilized cultured keratinocyte lysates
T Somers, L Duinslaeger, B Delaey, et al.
Acta Oto-Rhino-Laryngologica Belgica
|
July 4, 1998
The LAURA Pediatric Cochlear Implant Program in Antwerp: what have we learnt in 5 years?
F E Offeciers, P Govaerts, K Daemers, et al.
American Journal of Medical Genetics. Part A
|
October 17, 2008
Phenotypic consequences of a novel SCO2 gene mutation
Rob M Verdijk, Ronald de Krijger, Kees Schoonderwoerd, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
January 31, 2019
[Incidental detection of maternal malignancy in non-invasive prenatal test]
Lotte Saes, Lutgarde C P Govaerts, Maarten F C M Knapen, et al.
European Journal of Human Genetics : EJHG
|
November 7, 2013
Types of array findings detectable in cytogenetic diagnosis: a proposal for a generic classification
Malgorzata I Srebniak, Karin E M Diderich, Lutgarde C P Govaerts, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
July 31, 2013
Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature
M C de Wit, M I Srebniak, L C P Govaerts, et al.
Clinical Genetics
|
July 31, 2007
Exceptional good cognitive and phenotypic profile in a male carrying a mosaic mutation in the FMR1 gene
L C P Govaerts, A E Smit, J J Saris, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 10, 2015
Is prenatal cytogenetic diagnosis with genomic array indicated in pregnancies at risk for a molecular or metabolic disorder?
Malgorzata I Srebniak, Lutgarde C P Govaerts, Karin E M Diderich, et al.
Prenatal Diagnosis
|
July 15, 2011
Outcome of pregnancies complicated by oligohydramnios or anhydramnios of renal origin
E W M Grijseels, P T M Echteld van-Hornstra, L C P Govaerts, et al.
Page
of 9