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Human Genetics|January 5, 2001
Interchromosomal insertions. Identification of five cases and a reviewJ O Van Hemel, H J EussenClinical Genetics|March 1, 1975
Familial occurrence of the g syndromeJ P van Biervliet, J O van HemelPrenatal Diagnosis|September 1, 1993
Application of fluorescent in situ hybridization for 'de novo' anomalies in prenatal diagnosisD Van Opstal, H J Eussen, J O Van Hemel, et al.Journal of Medical Genetics|December 1, 1987
Interstitial del(13)(q21.3q31) associated with psychomotor retardation, eczema, and absent suck and swallowing reflexP J Peet, R R Pereira, J O Van Hemel, et al.American Journal of Medical Genetics|April 1, 1992
Limited size of the fragile X site shown by fluorescence in situ hybridizationA J Verkerk, B H Eussen, J O Van Hemel, et al.Human Genetics|March 1, 1992
Molecular detection of a translocation (Y;11) (q11.2;q24) in a 45,X male with signs of Jacobsen syndromeJ O Van Hemel, B Eussen, E Wesby-van Swaay, et al.Prenatal Diagnosis|February 1, 1987
Marker chromosomes in a series of 10,000 prenatal diagnoses. Cytogenetic and follow-up studiesE S Sachs, J O Van Hemel, J C Den Hollander, et al.Nederlands Tijdschrift Voor Geneeskunde|February 4, 1989
[Children with autism and related contact disorders: medical aspects]R B Minderaa, H Stroink, W Blom, et al.Obstetrics and Gynecology|March 1, 1985
Chromosome studies of 500 couples with two or more abortionsE S Sachs, M G Jahoda, J O Van Hemel, et al.Journal of Medical Genetics|January 1, 1994
De novo deletion (2) (p11.2p13): clinical, cytogenetic, and immunological dataF J Los, J O Van Hemel, H J Jacobs, et al.Pageof 4