A Marfan syndrome-like phenotype caused by a neocentromeric supernumerary ring chromosome 15

Clinical Impact of Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes

(2012) T. Liehr et al.   CYTOGENETIC AND GENOME RESEARCH

Mechanism and Genotype-Phenotype Correlation of Two Proximal 6q Deletions Characterized Using mBAND, FISH, Array CGH, and DNA Sequencing

(2011) M. Vlckova et al.   CYTOGENETIC AND GENOME RESEARCH

An unusual chromosome 22q11 deletion associated with an apparent complementary ring chromosome in a phenotypically normal woman

(2011) Jérôme Toutain et al.   European Journal of Medical Genetics

Meiotic Pairing Error in an Infertile Male Bearing Reciprocal Deletion of Chromosome 13

(2011) Y.-X. Cui et al.   JOURNAL OF ANDROLOGY

The revised Ghent nosology for the Marfan syndrome

(2010) B. L. Loeys et al.   JOURNAL OF MEDICAL GENETICS

Mechanisms and Consequences of Small Supernumerary Marker Chromosomes: From Barbara McClintock to Modern Genetic-Counseling Issues

(2008) Erin L. Baldwin et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Neocentromeres: New Insights into Centromere Structure, Disease Development, and Karyotype Evolution

(2008) Owen J. Marshall et al.   AMERICAN JOURNAL OF HUMAN GENETICS