1. De novo deletion (2) (p11.2p13): clinical, cytogenetic, and immunological data. Issue 1 (January 1994) Authors: Los, F J; Van Hemel, J O; Jacobs, H J; Drop, S L; van Dongen, J J Journal: Journal of medical genetics Issue: Volume 31:Issue 1(1994) Page Start: 72 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. First trimester diagnosis from chorionic villi of a der(15), t(9;15)(q33;q14)mat identified by DA/DAPI staining. Issue 1 (February 1986) Authors: Van Hemel, J O; Majoor-Krakauer, D F; Jahoda, M G; Sachs, E S Journal: Journal of medical genetics Issue: Volume 23:Issue 1(1986) Page Start: 89 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Interstitial del(13)(q21.3q31) associated with psychomotor retardation, eczema, and absent suck and swallowing reflex. Issue 12 (December 1987) Authors: Peet, P J; Pereira, R R; Van Hemel, J O; Hoogeboom, A J Journal: Journal of medical genetics Issue: Volume 24:Issue 12(1987) Page Start: 786 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Letter: Acute myelofibrosis and chromosome damage after procarbazine treatment. Issue 5929 (24th August 1974) Authors: Pinedo, H M; Van Hemel, J O; Vrede, M A; Van der Sluys Veer, J Journal: BMJ Issue: Volume 3:Issue 5929(1974) Page Start: 525 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Recurrence of DiGeorge syndrome: prenatal detection by FISH of a molecular 22q11 deletion. Issue 8 (August 1995) Authors: Van Hemel, J O; Schaap, C; Van Opstal, D; Mulder, M P; Niermeijer, M F; Meijers, J H Journal: Journal of medical genetics Issue: Volume 32:Issue 8(1995) Page Start: 657 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗