Academic Bibliography

Search 200 years of publications by Ghent University researchers.

prof. dr. Sandra Janssens

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Speech fluency in neurofibromatosis type 1

Marjan Cosyns (UGent) , Geert Mortier (UGent) , Sandra Janssens (UGent) , Nidhi Saharan (UGent) , Elien Stevens (UGent) and John Van Borsel (UGent)

(2010) JOURNAL OF FLUENCY DISORDERS. 35(1). p.59-69
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Speech disorders in neurofibromatosis type 1: a sample survey

Marjan Cosyns (UGent) , Lies Vandeweghe, Geert Mortier (UGent) , Sandra Janssens (UGent) and John Van Borsel (UGent)

(2010) INTERNATIONAL JOURNAL OF LANGUAGE & COMMUNICATION DISORDERS. 45(5). p.600-607
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- Conference Paper
- C3
Speech fluency in neurofibromatosis type 1

Marjan Cosyns (UGent) , Elien Stevens (UGent) , Nidhi Saharan (UGent) , Sandra Janssens (UGent) , Geert Mortier (UGent) and John Van Borsel (UGent)

(2009) 6th world congress on fluency disorders, Abstracts.
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- Journal Article
- A2
Het preconceptueel en prenataal advies

Sandra Janssens (UGent)

(2009) PATIENT CARE (BELGIE NEDERLANDSE ED.). p.5-10
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- Journal Article
- A1
Clinical and molecular genetic analysis of a family with macrothrombocytopenia and early onset sensorineural hearing loss

AN Mhatre, Sandra Janssens (UGent) , MA Nardi, Y Li and AK Lalwani

(2009) EUROPEAN JOURNAL OF MEDICAL GENETICS. 52(4). p.185-190
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- Journal Article
- A1
- open access
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome

BWM van Bon, HC Mefford, Björn Menten (UGent) , DA Koolen, AJ Sharp, WM Nillesen, JW Innis, TJL de Ravel, CL Mercer, M Fichera, et al.

(2009) JOURNAL OF MEDICAL GENETICS. 46(8). p.511-523
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- Journal Article
- A1
- open access
Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples

Björn Menten (UGent) , Katrien Swerts (UGent) , BARBARA DELLE CHIAIE (UGent) , Sandra Janssens (UGent) , Karen Buysse (UGent) , Jan Philippé (UGent) and Franki Speleman (UGent)

(2009) BMC MEDICAL GENETICS. 10.
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Whole body MR imaging in neurofibromatosis type 1

STEPHEN VAN MEERBEECK (UGent) , Koenraad Verstraete (UGent) , Sandra Janssens (UGent) and Geert Mortier (UGent)

(2009) EUROPEAN JOURNAL OF RADIOLOGY. 69(2). p.236-242
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- Journal Article
- A1
PRUNE BELLY ANOMALY ON PRENATAL ULTRASOUND AS A PRESENTING FEATURE OF ECTRODACTYLY-ECTODERMAL DYSPLASIA-CLEFTING SYNDROME (EEC)

Sandra Janssens (UGent) , Paul Defoort, C Vandenbroecke, H Scheffer and Geert Mortier (UGent)

(2008) GENETIC COUNSELING. 19(4). p.433-437
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NovelFGFR1 sequence variants in Kallmann syndrome, and genetic evidence that the FGFR1c isoform is required in olfactory bulb and palate morphogenesis

Catherine Dodé, Corinne Fouveaut, Geert Mortier (UGent) , Sandra Janssens (UGent) , Jérôme Bertherat, Jacques Mahoudeau, Marie-Laure Kottler, Christine Chabrolle, Antoine Gancel, Inge François, et al.

(2007) HUMAN MUTATION. 28(1). p.97-98

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