Ghent University Academic Bibliography

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Your filters: cql: author="Drop, SLS" or (type exact bookEditor and editor="Drop, SLS")

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Malignant testicular germ cell tumors in postpubertal individuals with androgen insensitivity : prevalence, pathology and relevance of single nucleotide polymorphism-based susceptibility profiling

Martine Cools (UGent) , KP Wolffenbuttel, R Hersmus, BB Mendonca, J Kaprova, SLS Drop, H Stoop, AJM Gillis, JW Oosterhuis, EMF Costa, et al.

(2017) HUMAN REPRODUCTION. 32(12). p.2561-2573
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Variable loss of functional activities of androgen receptor mutants in patients with androgen insensitivity syndrome

P Elfferich, ME Van Royen, DJ van den Wijngaart, J Trapman, SLS Drop, ELT van den Akker, SJ Lusher, R Bosch, T Bunch, IA Hughes, et al.

(2013) SEXUAL DEVELOPMENT. 7(5). p.223-234
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Pubertal androgenization and gonadal histology in two 46,XY adolescents with NR5A1 mutations and predominantly female phenotype at birth

Martine Cools (UGent) , Piet Hoebeke (UGent) , KP Wolffenbuttel, H Stoop, R Hersmus, M Barbaro, A Wedell, H Brüggenwirth, LHJ Looijenga and SLS Drop

(2012) EUROPEAN JOURNAL OF ENDOCRINOLOGY. 166(2). p.341-349
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Gonadal development and tumor formation at the crossroads of male and female sex determination

Martine Cools (UGent) , KP Wolffenbuttel, SLS Drop, JW Oosterhuis and LHJ Looijenga

(2011) SEXUAL DEVELOPMENT. 5(4). p.167-180
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Partial deletion of the NR5A1 (SF1) gene, detected by synthetic probe MLPA, in a patient with XY gonadal disorder of sex development

M Barbano, Martine Cools (UGent) , LHJ Looijenga, SLS Drop and A Wedell

(2011) SEXUAL DEVELOPMENT. 5(4). p.181-187
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Gonadal pathology and tumor risk in relation to clinical characteristics in patients with 45,X/46,XY mosaicism

Martine Cools (UGent) , J Pleskacova, H Stoop, Piet Hoebeke (UGent) , Erik Van Laecke (UGent) , SLS Drop, J Lebl, JW Oosterhuis, LHJ Looijenga and KP Wolffenbuttel

(2011) JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. 96(7). p.E1171-E1180
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Congenitale vaginale hypoplasie en psychosexueel functioneren: een huidige stand van zaken

Nina Callens (UGent) , GRETA DE CUYPERE (UGent) , KP Wolffenbuttel, SLS Drop, Piet Hoebeke (UGent) , Elien Van Hoecke, A Dessens and Martine Cools (UGent)

(2010) GUNAÏKEIA (NEDERLANDSE EDITIE). 15(8). p.286-290
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- Journal Article
- A2
- open access
Stoornissen in de geslachtsontwikkeling: Genetische basis, terminologie en het risico voor de ontwikkeling van kiemceltumoren.

Martine Cools (UGent) , LHJ Looijenga, KP Wolffenbuttel and SLS Drop

(2009) Tijdschrift voor geneeskunde. 65(16). p.709-722
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- Book Chapter
Genetic defects of female sexual differentiation

Arianne Dessens (UGent) , Martine Cools (UGent) , A Richter-Unruh, LHJ Looijenga, A Grootegoed and SLS Drop

(2009) Hormones, brain and behavior. p.3207-3234
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- Journal Article
- A2
Genetische basis, terminologie en het risico voor de ontwikkeling van kiemceltumoren bij stoornissen in de geslachtsontwikkeling

Martine Cools (UGent) , LHJ Looijenga, BJ Otten, KP Wolffenbuttel and SLS Drop

(2008) TIJDSCHRIFT VOOR KINDERGENEESKUNDE. 76(3). p.92-104

Academic Bibliography

Malignant testicular germ cell tumors in postpubertal individuals with androgen insensitivity : prevalence, pathology and relevance of single nucleotide polymorphism-based susceptibility profiling

Variable loss of functional activities of androgen receptor mutants in patients with androgen insensitivity syndrome

Pubertal androgenization and gonadal histology in two 46,XY adolescents with NR5A1 mutations and predominantly female phenotype at birth

Gonadal development and tumor formation at the crossroads of male and female sex determination

Partial deletion of the NR5A1 (SF1) gene, detected by synthetic probe MLPA, in a patient with XY gonadal disorder of sex development

Gonadal pathology and tumor risk in relation to clinical characteristics in patients with 45,X/46,XY mosaicism

Congenitale vaginale hypoplasie en psychosexueel functioneren: een huidige stand van zaken

Stoornissen in de geslachtsontwikkeling: Genetische basis, terminologie en het risico voor de ontwikkeling van kiemceltumoren.

Genetic defects of female sexual differentiation

Genetische basis, terminologie en het risico voor de ontwikkeling van kiemceltumoren bij stoornissen in de geslachtsontwikkeling

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