Distortion of female meiotic segregation and reduced male fertility in human Robertsonian translocations: Consistent with the centromere model of co-evolving centromere DNA/centromeric histone (CEMP-A)DANIEL, Art.American journal of medical genetics. 2002, Vol 111, Num 4, pp 450-452, issn 0148-7299Article

A series of supernumerary small ring marker autosomes identified by FISH with chromosome probe arrays and literature review excluding chromosome 15DANIEL, Art; MALAFIEJ, Paul.American journal of medical genetics. 2003, Vol 117A, Num 3, pp 212-222, issn 0148-7299, 11 p.Article

Three different origins for apparent triploid/diploid mosaicsDANIEL, Art; WU, Zhanhe; DARMANIAN, Artur et al.Prenatal diagnosis. 2003, Vol 23, Num 7, pp 529-534, issn 0197-3851, 6 p.Article

Isochromosome 5p mosaicism at prenatal diagnosis: observations and outcomes in six cases at chorionic villus sampling and one at amniocentesisWILSON, Susan Clement; SUSMAN, Marleen; BAIN, Sharon et al.Prenatal diagnosis. 2002, Vol 22, Num 8, pp 681-685, issn 0197-3851Article

Issues arising from the prenatal diagnosis of some rare trisomy mosaics: the importance of cryptic fetal mosaicismDANIEL, Art; ZHANHE WU; DARMANIAN, Artur et al.Prenatal diagnosis. 2004, Vol 24, Num 7, pp 524-536, issn 0197-3851, 13 p.Article

An innocuous duplication of 11.2 mb at 13q21 is gene poor : Sub-bands of gene paucity and pervasive CNV characterize the Chromosome anomaliesDANIEL, Art; DARMANIAN, Artur; PETERS, Greg et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 20, pp 2452-2459, issn 1552-4825, 8 p.Article

Molecular distinction between true centric fission and pericentric duplication-fissionPERRY, Jo; NOURI, Sara; PHUNG LA et al.Human genetics. 2005, Vol 116, Num 4, pp 300-310, issn 0340-6717, 11 p.Article

Recombinants of intrachromosomal transposition of subtelomeres in chromosomes 1 and 2: A cause of minute terminal chromosomal imbalancesDANIEL, Art; BAKER, Elizabeth; CHIA, Nicole et al.American journal of medical genetics. 2003, Vol 117A, Num 1, pp 57-64, issn 0148-7299, 8 p.Article

Chromosome 13q neocentromeres: Molecular cytogenetic characterization of three additional cases and clinical spectrumSHULAN LI; MALAFIEJ, Paul; VELAGALETI, Golpalrao V. N et al.American journal of medical genetics. 2002, Vol 110, Num 3, pp 258-267, issn 0148-7299Article

Karyotype, phenotype and parental origin in 19 cases of triploidyDANIEL, Art; ZHANHE WU; LOO, Christine et al.Prenatal diagnosis. 2001, Vol 21, Num 12, pp 1034-1048, issn 0197-3851Article

A case of maternal uniparental disomy of chromosome 9 diagnosed prenatally and the related problem of residual trisomySLATER, Howard R; RALPH, Adrianne; DANIEL, Art et al.Prenatal diagnosis. 2000, Vol 20, Num 11, pp 930-932, issn 0197-3851Article