First trimester diagnosis from chorionic villi of a der(15),t(9;15)(q33;q14)mat identified by DA/DAPI staining.

Por Van Hemel, J O, Majoor-Krakauer, D F, Jahoda, M G, Sachs, E S
Publicado em 1986

Interstitial del(13)(q21.3q31) associated with psychomotor retardation, eczema, and absent suck and swallowing reflex.

Por Peet, P J, Pereira, R R, Van Hemel, J O, Hoogeboom, A J
Publicado em 1987

Letter: Acute myelofibrosis and chromosome damage after procarbazine treatment.

Por Pinedo, H M, Van Hemel, J O, Vrede, M A, Van der Sluys Veer, J
Publicado em 1974

De novo deletion (2) (p11.2p13): clinical, cytogenetic, and immunological data.

Por Los, F J, Van Hemel, J O, Jacobs, H J, Drop, S L, van Dongen, J J
Publicado em 1994

Recurrence of DiGeorge syndrome: prenatal detection by FISH of a molecular 22q11 deletion.

Por Van Hemel, J O, Schaap, C, Van Opstal, D, Mulder, M P, Niermeijer, M F, Meijers, J H
Publicado em 1995

Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.

Por de Vries, B B, Fryns, J P, Butler, M G, Canziani, F, Wesby-van Swaay, E, van Hemel, J O, Oostra, B A, Halley, D J, Niermeijer, M F
Publicado em 1993

An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito

Por Eussen, B., Bartalini, G., Bakker, L., Balestri, P., Di, L, Van Hemel, J. O, Dauwerse, H., van den Ouweland, A. M W, Ris-Stalpers, C., Verhoef, S., Halley, D., Fois, A.
Publicado em 2000

Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndrome.

Por Meijers-Heijboer, E J, Sandkuijl, L A, Brunner, H G, Smeets, H J, Hoogeboom, A J, Deelen, W H, van Hemel, J O, Nelen, M R, Smeets, D F, Niermeijer, M F
Publicado em 1992

Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family.

Por de Vries, B B, Jansen, C C, Duits, A A, Verheij, C, Willemsen, R, van Hemel, J O, van den Ouweland, A M, Niermeijer, M F, Oostra, B A, Halley, D J
Publicado em 1996

Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere.

Por Warburton, P E, Dolled, M, Mahmood, R, Alonso, A, Li, S, Naritomi, K, Tohma, T, Nagai, T, Hasegawa, T, Ohashi, H, Govaerts, L C, Eussen, B H, Van Hemel , J O, Lozzio, C, Schwartz, S, Dowhanick-Morrissette, J J, Spinner, N B, Rivera, H, Crolla, J A, Yu, C, Warburton, D
Publicado em 2000