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Journal of Medical Genetics|December 10, 1997
Misleading linkage results in an NF2 presymptomatic test owing to mosaicismE K Bijlsma, A J Wallace, D G EvansPrenatal Diagnosis|January 22, 2005
Increased nuchal translucency and split-hand/foot malformation in a fetus with an interstitial deletion of chromosome 2q that removes the SHFM5 locusE K Bijlsma, A C Knegt, C M Bilardo, et al.European Journal of Pediatrics|July 31, 2001
Neurofibromatosis type 2 diagnosed in the absence of vestibular schwannomas. A case report and guidelines for a screening protocol for children at riskA J Janse, W F Tan, C B Majoie, et al.Genes, Chromosomes & Cancer|February 1, 1994
Amplification of the anonymous marker D17S67 in malignant astrocytomasE K Bijlsma, S Leenstra, A Westerveld, et al.Genes, Chromosomes & Cancer|October 1, 1992
Molecular characterization of chromosome 22 deletions in schwannomasE K Bijlsma, R Brouwer-Mladin, D A Bosch, et al.Prenatal Diagnosis|March 11, 2003
Prenatal diagnosis of a karyotypically normal pregnancy in a mother with a supernumerary neocentric 13q21 -->13q22 chromosome and balancing reciprocal deletionA C Knegt, S Li, J J M Engelen, et al.Cytogenetics and Cell Genetics|January 1, 1991
Direct assignment of the human beta B2 and beta B3 crystallin genes to 22q11.2----q12: markers for neurofibromatosis 2T J Hulsebos, E K Bijlsma, A H Geurts van Kessel, et al.Genes, Chromosomes & Cancer|September 1, 1994
Analysis of mutations in the SCH gene in schwannomasE K Bijlsma, P Merel, D A Bosch, et al.British Journal of Cancer|October 1, 1994
Allele loss on chromosomes 10 and 17p and epidermal growth factor receptor gene amplification in human malignant astrocytoma related to prognosisS Leenstra, E K Bijlsma, D Troost, et al.Clinical Dysmorphology|August 24, 1999
A patient with a de novo t (6;9) and an interstitial duplication of (9)(q21.2q22.1)M F Mohrschladt, E K Bijlsma, S Sluijter, et al.Pageof 3