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Books
Empty and full : the language of Chinese painting / François Cheng ; translated by Michael H. Kohn.
Author / Creator:Cheng, François, 1929-
Publisher:Boston : Shambhala : Distributed in the United States by Random House, 1994.
Edition:1st ed.
Date:1994.
Call Numbers:N759.951/13
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Maps
Carte reduite des terres Australes pour servir a l'histoire des voyages [cartographic material] / par le sr. Bellin ing. de la marine de la Societé Royale de Londres &ca.
Author / Creator:Bellin, Jacques Nicolas, 1703-1772.
Publisher:[Londres], 1753 ; [Christchurch, N.Z.] : Avon Fine Prints, 1970.
Date:1753 ; 1970.
Call Numbers:M2 800/1753/3 , M2 800/1753/2
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Maps
Carte réduite des terres Australes pour servir a l'histoire des voyages [cartographic material] / par le Sr. Bellin, Ing. de la marine de la Societé Royale de Londres & ca. 1753.
Author / Creator:Bellin, Jacques Nicolas, 1703-1772.
Publisher:Canberra : Australian Institute of Cartographers, A.C.T. Division, 1985.
Date:1985.
Call Numbers:MA2 800/1753/5 , M2 800/1753/5
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Intellectuals and tradition / edited by S. N. Eisenstadt and S. R. Graubard.
Author / Creator:Eisenstadt, S. N. (Shmuel Noah), 1923- comp.
Publisher:New York : Humanities Press, [c1973]
Date:[c1973]
Call Numbers:T0185137
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Maps
Carte réduite des terres Australes [cartographic material] : pour servir a l'Histoire des voyages / par Le Sr. Bellin Ing, de la Marine de la Societé Royale de Londres & ca. 1753.
Author / Creator:Bellin, Jacques Nicolas, 1703-1772.
Publisher:[A Paris : Chez Didot, 1753]
Date:1753]
Call Numbers:M2 800/1753/1 , Z/M2 800/1753/1
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ArticlesPeer ReviewedFull Text
PREPL deficiency: delineation of the phenotype and development of a functional blood assay
Author / Creator:Régal, Luc ; Mårtensson, Emma ; Maystadt, Isabelle ; Voermans, Nicol ; Lederer, Damien ; Burlina, Alberto ; Juan Fita, María Jesús ; Hoogeboom, A. Jeannette M. ; Olsson Engman, Mia ; Hollemans, Tess ; Schouten, Meyke ; Meulemans, Sandra ; Jonson, Tord ; François, Inge ; Gil Ortega, David ; Kamsteeg, Erik-Jan ; Creemers, John W.M.
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2018-01, Vol.20 (1), p.109-118
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ArticlesPeer ReviewedFull Text
Cardiovascular pathology in males and females with 45,X/46,XY mosaicism
Author / Creator:De Groote, Katya ; Cools, Martine ; De Schepper, Jean ; Craen, Margarita ; François, Inge ; Devos, Daniel ; Carbonez, Karlien ; Eyskens, Benedicte ; De Wolf, Daniel
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-02, Vol.8 (2), p.e54977-e54977
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ArticlesPeer ReviewedFull Text
Profiling of conserved non-coding elements upstream of SHOX and functional characterisation of the SHOX cis-regulatory landscape
Author / Creator:Verdin, Hannah ; Fernández-Miñán, Ana ; Benito-Sanz, Sara ; Janssens, Sandra ; Callewaert, Bert ; De Waele, Kathleen ; De Schepper, Jean ; François, Inge ; Menten, Björn ; Heath, Karen E. ; Gómez-Skarmeta, José Luis ; De Baere, Elfride
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2015-12, Vol.5 (1), p.17667-17667, Article 17667
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ArticlesPeer ReviewedFull Text
Global distribution of the most prevalent deletions causing hypotonia–cystinuria syndrome
Author / Creator:Martens, Kevin ; Heulens, Inge ; Meulemans, Sandra ; Zaffanello, Marco ; Tilstra, David ; Hes, Frederik J ; Rooman, Raoul ; François, Inge ; de Zegher, Francis ; Jaeken, Jaak ; Matthijs, Gert ; Creemers, John W M
Publisher:Cham: Springer International Publishing
Journal title:European journal of human genetics : EJHG, 2007-10, Vol.15 (10), p.1029-1033
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ArticlesPeer ReviewedFull Text
Novel FGFR1 sequence variants in Kallmann syndrome, and genetic evidence that the FGFR1c isoform is required in olfactory bulb and palate morphogenesis
Author / Creator:Dodé, Catherine ; Fouveaut, Corinne ; Mortier, Geert ; Janssens, Sandra ; Bertherat, Jérôme ; Mahoudeau, Jacques ; Kottler, Marie-Laure ; Chabrolle, Christine ; Gancel, Antoine ; François, Inge ; Devriendt, Koen ; Wolczynski, Slawomir ; Pugeat, Michel ; Pineiro-Garcia, Alfons ; Murat, Arnaud ; Bouchard, Philippe ; Young, Jacques ; Delpech, Marc ; Hardelin, Jean-Pierre
Publisher:Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 2007-01, Vol.28 (1), p.97-98
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ArticlesPeer ReviewedFull Text
Psychosocial Functioning, Self-Perception and Body Image and Their Auxologic Correlates in Growth Hormone and Oestrogen-Treated Young Adult Women with Turner Syndrome
Author / Creator:Lagrou, Katrien ; Froidecoeur, Christelle ; Verlinde, Francisca ; Craen, Margaretha ; De Schepper, Jean ; François, Inge ; Massa, Guy
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Hormone research in paediatrics, 2006-01, Vol.66 (6), p.277-284
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ArticlesPeer ReviewedFull Text
Methylation defect in imprinted genes detected in patients with an Albright's hereditary osteodystrophy like phenotype and platelet Gs hypofunction
Author / Creator:Izzi, Benedetta ; Francois, Inge ; Labarque, Veerle ; Thys, Chantal ; Wittevrongel, Christine ; Devriendt, Koen ; Legius, Eric ; Van den Bruel, Annick ; D'Hooghe, Marc ; Lambrechts, Diether ; de Zegher, Francis ; Van Geet, Chris ; Freson, Kathleen
Publisher:United States: Public Library of Science
Journal title:PloS one, 2012-06, Vol.7 (6), p.e38579-e38579
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ArticlesPeer ReviewedFull Text
Insulin Sensitivity Modulates the Growth Response during the First Year of High-Dose Growth Hormone Treatment in Short Prepubertal Children Born Small for Gestational Age
Author / Creator:Gies, Inge ; Thomas, Muriel ; Tenoutasse, Sylvie ; De Waele, Kathleen ; Lebrethon, Marie-Christine ; Beckers, Dominique ; Francois, Inge ; Maes, Marc ; Rooman, Raoul ; de Beaufort, Carine ; Massa, Guy ; De Schepper, Jean
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Hormone research in paediatrics, 2012-01, Vol.78 (1), p.24-30
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ArticlesPeer ReviewedFull Text
No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activity
Author / Creator:Izzi, Benedetta ; de Zegher, Francis ; Francois, Inge ; del Favero, Jurgen ; Goossens, Dirk ; Wittevrongel, Christine ; Thys, Chantal ; Van Geet, Chris ; Freson, Kathleen
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2012-04, Vol.57 (4), p.277-279
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ArticlesPeer ReviewedFull Text
NovelFGFR1 sequence variants in Kallmann syndrome, and genetic evidence that the FGFR1c isoform is required in olfactory bulb and palate morphogenesis
Author / Creator:Dodé, Catherine ; Fouveaut, Corinne ; Mortier, Geert ; Janssens, Sandra ; Bertherat, Jérôme ; Mahoudeau, Jacques ; Kottler, Marie-Laure ; Chabrolle, Christine ; Gancel, Antoine ; François, Inge ; Devriendt, Koen ; Wolczynski, Slawomir ; Pugeat, Michel ; Pineiro-Garcia, Alfons ; Murat, Arnaud ; Bouchard, Philippe ; Young, Jacques ; Delpech, Marc ; Hardelin, Jean-Pierre
Journal title:Human mutation, 2007-01, Vol.28 (1), p.97-98
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ArticlesPeer ReviewedFull Text
Detailed studies of growth hormone secretion in cystinosis patients
Author / Creator:Besouw, Martine T. P. ; Van Dyck, Maria ; Francois, Inge ; Van Hoyweghen, Elke ; Levtchenko, Elena N.
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Pediatric nephrology (Berlin, West), 2012-11, Vol.27 (11), p.2123-2127
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ArticlesPeer ReviewedFull Text
Has the Prevalence of Congenital Abnormalities after Intracytoplasmic Sperm Injection Increased? The Leuven Data 1994–2000 and a Review of the Literature
Author / Creator:Hindryckx, An ; Peeraer, Karen ; Debrock, Sophie ; Legius, Eric ; de Zegher, Francis ; Francois, Inge ; Vanderschueren, Dirk ; Demyttenaere, Koen ; Rijkers, Anna ; D’Hooghe, Thomas
Publisher:Basel, Switzerland: Karger
Journal title:Gynecologic and obstetric investigation, 2010-01, Vol.70 (1), p.11-22
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Global distribution of the most prevalent deletions causing hypotonia-cystinuria syndrome. Commentary
Author / Creator:PARVARI, Ruti ; HERSHKOVITZ, Eli ; DE ZEGHER, Francis ; JAEKEN, Jaak ; MATTHIJS, Gert ; CREEMERS, John W. M ; MARTENS, Kevin ; HEULENS, Inge ; MEULEMANS, Sandra ; ZAFFANELLO, Marco ; TILSTRA, David ; HES, Frederik J ; ROOMAN, Raoul ; FRANCOIS, Inge
Publisher:Avenel, NJ: Nature Publishing
Journal title:European journal of human genetics : EJHG, 2007, Vol.15 (10)
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ArticlesPeer ReviewedFull Text
Growth Hormone (GH) Secretion in Patients with Childhood-Onset GH Deficiency: Retesting after One Year of Therapy and at Final Height
Author / Creator:Thomas, M. ; Massa, G. ; Maes, M. ; Beckers, D. ; Craen, M. ; François, I. ; Heinrichs, C. ; Bourguignon, J.-P.
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Hormone research in paediatrics, 2003-01, Vol.59 (1), p.7-15
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ArticlesPeer ReviewedFull Text
Androgens and Fetal Growth
Author / Creator:de Zegher, Francis ; Francois, Inge ; Boehmer, Annemie L.M. ; Saggese, Giuseppe ; Müller, Jørn ; Hiort, Olaf ; Sultan, Charles ; Clayton, Peter ; Brauner, Raja ; Cacciari, Emanuele ; Ibáñez, Lourdes ; van Vliet, Guy ; Tiulpakov, Anatoly ; Saka, Nurçin ; Ritzén, Martin ; Sippell, Wolfgang G. ; Androgens and Fetal Growth Study Group, A
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Hormone research in paediatrics, 1998, Vol.50 (4), p.243-244
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Empty and full : the language of Chinese painting / François Cheng ; translated by Michael H. Kohn.

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Carte reduite des terres Australes pour servir a l'histoire des voyages [cartographic material] / par le sr. Bellin ing. de la marine de la Societé Royale de Londres &ca.

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Carte réduite des terres Australes pour servir a l'histoire des voyages [cartographic material] / par le Sr. Bellin, Ing. de la marine de la Societé Royale de Londres & ca. 1753.

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Intellectuals and tradition / edited by S. N. Eisenstadt and S. R. Graubard.

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Carte réduite des terres Australes [cartographic material] : pour servir a l'Histoire des voyages / par Le Sr. Bellin Ing, de la Marine de la Societé Royale de Londres & ca. 1753.

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PREPL deficiency: delineation of the phenotype and development of a functional blood assay

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Cardiovascular pathology in males and females with 45,X/46,XY mosaicism

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Profiling of conserved non-coding elements upstream of SHOX and functional characterisation of the SHOX cis-regulatory landscape

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Global distribution of the most prevalent deletions causing hypotonia–cystinuria syndrome

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Novel FGFR1 sequence variants in Kallmann syndrome, and genetic evidence that the FGFR1c isoform is required in olfactory bulb and palate morphogenesis

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Psychosocial Functioning, Self-Perception and Body Image and Their Auxologic Correlates in Growth Hormone and Oestrogen-Treated Young Adult Women with Turner Syndrome

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Methylation defect in imprinted genes detected in patients with an Albright's hereditary osteodystrophy like phenotype and platelet Gs hypofunction

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Insulin Sensitivity Modulates the Growth Response during the First Year of High-Dose Growth Hormone Treatment in Short Prepubertal Children Born Small for Gestational Age

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No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activity

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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

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Detailed studies of growth hormone secretion in cystinosis patients

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Has the Prevalence of Congenital Abnormalities after Intracytoplasmic Sperm Injection Increased? The Leuven Data 1994–2000 and a Review of the Literature

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Global distribution of the most prevalent deletions causing hypotonia-cystinuria syndrome. Commentary

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Growth Hormone (GH) Secretion in Patients with Childhood-Onset GH Deficiency: Retesting after One Year of Therapy and at Final Height

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Androgens and Fetal Growth

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