Molecular characterization of 39de novosSMC: contribution to prognosis and genetic counselling, a prospective study

Supernumerary marker chromosomes derived from chromosome 6: Cytogenetic, molecular cytogenetic, and array CGH characterization

(2012) Bing Huang et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies

(2012) C-N Lee et al.   BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY

A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity

(2012) Kavita S. Reddy et al.   GENETICS IN MEDICINE

Genomic characterization of prenatally detected chromosomal structural abnormalities using oligonucleotide array comparative genomic hybridization

(2011) Peining Li et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Characterization of sSMC by FISH and molecular techniques

(2011) Frenny Sheth et al.   European Journal of Medical Genetics

Normal prenatal ultrasound findings in a case withde novomosaic small supernumerary marker chromosome 18 – how to counsel?

(2011) Christel Eckmann-Scholz et al.   Journal of Maternal-Fetal & Neonatal Medicine

Small supernumerary marker chromosome originating from chromosome 10 associated with an apparently normal phenotype

(2009) Pi-Lin Sung et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

High resolution SNP based microarray mapping of mosaic supernumerary marker chromosomes 13 and 17: Delineating novel loci for apraxia

(2009) Jillene M. Kogan et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Detection of an interstitial 3q21.1-q21.3 deletion in a child with multiple congenital abnormalities, mental retardation, pancytopenia, and myelodysplasia

(2009) P. Callier et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Molecular Cytogenetic Characterization of Two Cases with de novo Small Mosaic Supernumerary Marker Chromosomes Derived from Chromosome 16: Towards a Genotype/Phenotype Correlation

(2009) J.B. Melo et al.   CYTOGENETIC AND GENOME RESEARCH

Handling small supernumerary marker chromosomes in prenatal diagnostics

(2009) Thomas Liehr et al.   EXPERT REVIEW OF MOLECULAR DIAGNOSTICS

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

Supernumerary marker chromosomes management in prenatal diagnosis

(2008) Nicolas Gruchy et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Array-CGH in a series of 30 patients with mental retardation, dysmorphic features, and congenital malformations detected an interstitial 1p22.2-p31.1 deletion in a patient with features overlapping the Goldenhar syndrome

(2008) P. Callier et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Analphoid supernumerary marker chromosome characterized by aCGH and FISH as inv dup(3)(q25.33qter) de novo in a child with dysmorphic features and streaky pigmentation: case report

(2008) Sabita K Murthy et al.   Molecular Cytogenetics

Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridization

(2008) Karen D Tsuchiya et al.   Molecular Cytogenetics