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

le Van Hemel, J O, Majoor-Krakauer, D F, Jahoda, M G, Sachs, E S
Foilsithe 1986

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

le Peet, P J, Pereira, R R, Van Hemel, J O, Hoogeboom, A J
Foilsithe 1987

Letter: Acute myelofibrosis and chromosome damage after procarbazine treatment.

le Pinedo, H M, Van Hemel, J O, Vrede, M A, Van der Sluys Veer, J
Foilsithe 1974

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

le Los, F J, Van Hemel, J O, Jacobs, H J, Drop, S L, van Dongen, J J
Foilsithe 1994

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

le Van Hemel, J O, Schaap, C, Van Opstal, D, Mulder, M P, Niermeijer, M F, Meijers, J H
Foilsithe 1995

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

le 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
Foilsithe 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

le 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.
Foilsithe 2000

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

le 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
Foilsithe 1992

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

le 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
Foilsithe 1996

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

le 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
Foilsithe 2000