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Results:
1-14
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Results: 14
Authors:
Schuring-Blom, GH
Hoovers, JMN
van Lith, JMM
Knegt, AD
Leschot, NJ
Citation: Gh. Schuring-blom et al., FISH analysis of fetal nucleated red blood cells from CVS washings in cases of aneuploidy, PRENAT DIAG, 21(10), 2001, pp. 864-867
Authors:
Kleefstra, T
van de Zande, G
Merkx, G
Mieloo, H
Hoovers, JMN
Smeets, D
Citation: T. Kleefstra et al., Identification of an unbalanced cryptic translocation between the chromosomes 8 and 13 in two sisters with mild mental retardation accompanied by mild dysmorphic features, EUR J HUM G, 8(8), 2000, pp. 637-640
Authors:
Maas, SM
Hoovers, JMN
van Seggelen, ME
Menzel, DM
Hennekam, RCM
Citation: Sm. Maas et al., Interstitial deletion of the long arm of chromosome 2: a clinically recognizable microdeletion syndrome?, CLIN DYSMOR, 9(1), 2000, pp. 47-53
Authors:
Saxena, R
de Vries, JWA
Repping, S
Alagappan, RK
Skaletsky, H
Brown, LG
Ma, P
Chen, ES
Hoovers, JMN
Page, DC
Citation: R. Saxena et al., Four DAZ genes in two clusters found in the AZFc region od the human Y chromosome, GENOMICS, 67(3), 2000, pp. 256-267
Authors:
Jakobs, ME
van Lith, JMM
de Graaf, IM
Knegt, AC
Hoovers, JMN
Citation: Me. Jakobs et al., Genetic analysis of fetal nucleated red blood cells from CVS washings, PRENAT DIAG, 20(10), 2000, pp. 832-834
Authors:
Grierson, AJ
van Groenigen, M
Groot, NPB
Lindblad, K
Hoovers, JMN
Schalling, M
de Belleroche, J
Baas, F
Citation: Aj. Grierson et al., An integrated map of chromosome 18 CAG trinucleotide repeat loci, EUR J HUM G, 7(1), 1999, pp. 12-19
Authors:
Mohrschladt, MF
Bijlsma, EK
Sluijter, S
De Coo, RFM
Hoovers, JMN
Leschot, NJ
Citation: Mf. Mohrschladt et al., A patient with a de novo t(6;9) and an interstitial duplication of (9)(q21.2q22.1), CLIN DYSMOR, 8(3), 1999, pp. 211-214
Authors:
Schalk, JAC
Offenberg, HH
Peters, E
Groot, NPB
Hoovers, JMN
Heyting, C
Citation: Jac. Schalk et al., Isolation and characterization of the human SCP2 cDNA and chromosomal localization of the gene, MAMM GENOME, 10(6), 1999, pp. 642-644
Authors:
de Graaf, IM
Jakobs, ME
Leschot, NJ
Ravkin, I
Goldbard, S
Hoovers, JMN
Citation: Im. De Graaf et al., Enrichment, identification and analysis of fetal cells from maternal blood: Evaluation of a prenatal diagnosis system, PRENAT DIAG, 19(7), 1999, pp. 648-652
Authors:
de Graaf, IM
van Bezouw, SMCA
Jakobs, ME
Leschot, NJ
Zondervan, HA
Bilardo, CM
Hoovers, JMN
Citation: Im. De Graaf et al., First-trimester non-invasive prenatal diagnosis of triploidy, PRENAT DIAG, 19(2), 1999, pp. 175-177
Authors:
Aalfs, CM
Hoovers, JMN
Wijburg, FA
Citation: Cm. Aalfs et al., Molecular analysis of a translocation (6;11)(p21;q25) in a girl with Jacobsen syndrome, AM J MED G, 86(4), 1999, pp. 398-400
Authors:
Bijlsma, EK
Aalfs, CM
Sluijter, S
Luttikhuis, MEMO
Trembath, RC
Hoovers, JMN
Hennekam, RCM
Citation: Ek. Bijlsma et al., Familial cryptic translocation between chromosomes 2qter and 8qter: further delineation of the Albright hereditary osteodystrophy-like phenotype, J MED GENET, 36(8), 1999, pp. 604-609
Authors:
Groen, SE
Drewes, JG
de Boer, EG
Hoovers, JMN
Hennekam, RCM
Citation: Se. Groen et al., Repeated unbalanced offspring due to a familial translocation involving chromosomes 5 and 6, AM J MED G, 80(5), 1998, pp. 448-453
Authors:
Meijer, GA
Hermsen, MAJA
Baak, JPA
van Diest, PJ
Meuwissen, SGM
Belien, JAM
Hoovers, JMN
Joenje, H
Snijders, PJF
Walboomers, JMM
Citation: Ga. Meijer et al., Progression from colorectal adenoma to carcinoma is associated with non-random chromosomal gains as detected by comparative genomic hybridisation, J CLIN PATH, 51(12), 1998, pp. 901-909
Risultati:
1-14
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