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Author/Creator Peeters, Hilde

2. A complex Xp11.22 deletion in a patient with syndromic autism: Exploration of FAM120C as a positional candidate gene for autism. Issue 12 (24th September 2014)

Authors:
De Wolf, Veerle; Crepel, An; Schuit, Frans; van Lommel, Leentje; Ceulemans, Berten; Steyaert, Jean; Seuntjens, Eve; Peeters, Hilde; Devriendt, Koen
Journal:
American journal of medical genetics
Issue:
Volume 164:Issue 12(2014.)
Page Start:
3035
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. A comprehensive clinical and genetic study in 127 patients with ID in Kinshasa, DR Congo. Issue 9 (8th August 2018)

Authors:
Lumaka, Aimé; Race, Valerie; Peeters, Hilde; Corveleyn, Anniek; Coban‐Akdemir, Zeynep; Jhangiani, Shalini N.; Song, Xiaofei; Mubungu, Gerrye; Posey, Jennifer; Lupski, James R.; Vermeesch, Joris R.; Lukusa, Prosper; Devriendt, Koenraad
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 9(2018)
Page Start:
1897
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. A de-novo 15q24.2 deletion involving SIN3A is associated with emotional, behavioural, motor problems and hypersensitivity in a girl with above average intelligence and typical facial features. Issue 4 (October 2020)

Authors:
Sleyp, Yoeri; Swillen, Ann; Van Den Bogaert, Kris; Massa, Guy; Aerssens, Peter; Peeters, Hilde
Journal:
Clinical dysmorphology
Issue:
Volume 29:Issue 4(2020:Oct.)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

5. Accuracy and Clinical Value of Maternal Incidental Findings During Noninvasive Prenatal Testing for Fetal Aneuploidies. Issue 8 (August 2017)

Authors:
Brison, Nathalie; van den Bogaert, Kris; Dehaspe, Luc; van den Oever, Jessica M. E.; Janssens, Katrien; Blaumeiser, Bettina; Peeters, Hilde; van Esch, Hilde; van Buggenhout, Griet; Vogels, Annick; de Ravel, Thomy; Legius, Eric; Devriendt, Koen; Vermeesch, Joris R.
Journal:
Obstetrical & gynecological survey
Issue:
Volume 72:Issue 8(2017)
Page Start:
Record Type:
Journal Article
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7. CREBBP mutations in individuals without Rubinstein–Taybi syndrome phenotype. Issue 10 (17th June 2016)

Authors:
Menke, Leonie A.; van Belzen, Martine J.; Alders, Marielle; Cristofoli, Francesca; Ehmke, Nadja; Fergelot, Patricia; Foster, Alison; Gerkes, Erica H.; Hoffer, Mariëtte J. V.; Horn, Denise; Kant, Sarina G.; Lacombe, Didier; Leon, Eyby; Maas, Saskia M.; Melis, Daniela; Muto, Valentina; Park, Soo‐Mi...
Other Names:
Hennekam Raoul C.M. guestEditor.; Biesecker Leslie G. guestEditor.
Journal:
American journal of medical genetics
Issue:
Volume 170:Issue 10(2016)
Page Start:
2681
Record Type:
Journal Article
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9. Exploring informed choice in preconception reproductive genetic carrier screening by using a modified Multidimensional Measure of Informed Choice. Issue 11 (November 2022)

Authors:
Van Steijvoort, Eva; Peeters, Hilde; Vandecruys, Hilde; Verguts, Jasper; Peeraer, Karen; Matthijs, Gert; Borry, Pascal
Journal:
Patient education and counseling
Issue:
Volume 105:Issue 11(2022)
Page Start:
3313
Record Type:
Journal Article
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