• A case of familial central precocious puberty caused by a novel mutation in the makorin RING finger protein 3 gene
• A case of mosaic supernumerary ring chromosome 15 with two copies of the segment 15p11.1-q14
• A case of ring chromosome 15 accompanied by almost normal intelligence
• A common genetic variant in the 15q24 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) is associated with a reduced ability of women to quit smoking in pregnancy
• A Familial Small Supernumerary Marker Chromosome 15 Associated with Cryptic Mosaicism with Two Different Additional Marker Chromosomes Derived de novo from Chromosome 9: Detailed Case Study and Implications for Recurrent Pregnancy Loss
• A FURTHER PATIENT OF PURE 15q DELETION: CLINICAL AND MOLECULAR CYTOGENETIC FINDINGS
• A girl with cutaneous hyperpigmentation, café au lait spots and ring chromosome 15 without significant deletion
• A Marfan syndrome-like phenotype caused by a neocentromeric supernumerary ring chromosome 15
• A novel aberration of COL1A1-PDGFB fusion as an insertion in chromosome 15 in one case of dermatofibrosarcoma protuberans involving a rare location
• A patient with Prader-Willi syndrome and a supernumerary marker chromosome r(15)(q11.1-13p11.1)pat and maternal heterodisomy
• A series of supernumerary small ring marker autosomes identified by FISH with chromosome probe arrays and literature review excluding chromosome 15
• A somatic origin of homologous Robertsonian translocations and isochromosomes
• Aggressive embryonal rhabdomyosarcoma in a 3-month-old boy: A clinical and molecular analysis
• An infant with deletion of the distal long arm of chromosome 15 (q26.1----qter) and loss of insulin-like growth factor 1 receptor gene
• Apparent Prader-Willi phenotype in a woman with ring chromosome 9
• Association between acute promyelocytic leukemia and ring chromosome 6
• Autism and maternally derived aberrations of chromosome 15q
• Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3
• Characterisation of the PML/RAR alpha rearrangement associated with t(15;17) acute promyelocytic leukaemia
• Chromosomal abnormalities in 2 cases of testicular failure
• Chromosomal rearrangements in patients with clinical features of Silver-Russell syndrome
• Chromosome 15
• Chromosome 15 structural abnormalities: effect on <em>IGF1R</em> gene expression and function
• Clinical, cytogenetic and molecular analyses of a rare case with ring chromosome 15 and review of the literature
• Clonality and methylation status of the Epstein-Barr virus (EBV) genomes in in vivo-infected EBV-carrying chronic lymphocytic leukemia (CLL) cell lines
• Combined spectral karyotyping and microarray-based comparative genomic hybridization for the diagnosis of a case with ring chromosome 15
• Constitutional abnormalities of chromosome 21 predispose to iAMP21-acute lymphoblastic leukaemia
• Copy number changes and methylation patterns in an isodicentric and a ring chromosome of 15q11-q13: report of two cases and review of literature
• Cutis tricolor parvimaculata in ring chromosome 15 syndrome: A case report
• Cutis tricolor parvimaculata in two patients with ring chromosome 15 syndrome
• De Novo Ring Chromosome 15: Molecular Cytogenetic and Clinical Characterization of First Case from Saudi Arabia
• Decreased cell viability of fibroblasts from two patients with a ring chromosome: an in vitro reflection of growth failure?
• Detection of a patient with ring chromosome 15 by low-coverage massively parallel copy number variation sequencing
• Direct outgrowth of in vivo Epstein-Barr virus (EBV)-infected chronic lymphocytic leukemia (CLL) cells into permanent lines
• Distinct 15q genotypes in Russell-Silver and ring 15 syndromes
• Dysplastic features, growth retardation, malrotation of the gut, and fatal ventricular septal defect in a 4-month-old girl with ring chromosome 15
• Familial occurrence of ring chromosome 15
• Familial supernumerary marker chromosome evolution through three generations
• Fecundity in an infertile man with r(15) - a challenge to the current paradigm
• Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization
• FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosomes 15 and 22: I. Results of 26 new cases
• FISH characterization of small supernumerary marker chromosomes in two Prader-Willi patients
• Genetic determinants of susceptibility to silver nanoparticle-induced acute lung inflammation in mice
• GENETICS IN ENDOCRINOLOGY: Genetic etiologies of central precocious puberty and the role of imprinted genes
• Good growth response to growth hormone treatment in the ring chromosome 15 syndrome
• Hemizygosity at the insulin-like growth factor I receptor (IGF1R) locus and growth failure in the ring chromosome 15 syndrome
• In vitro and in vivo responses to short-term recombinant human insulin-like growth factor-1 (IGF-I) in a severely growth-retarded girl with ring chromosome 15 and deletion of a single allele for the type 1 IGF receptor gene
• Increased fetal nuchal fold leading to prenatal diagnosis of ring chromosome 15
• Kidney abnormalities in persons with monosomy 15q26
• Mammary analog secretory carcinoma of salivary gland: cytologic diagnosis and differential diagnosis of an unreported entity
• Maternal transmission of a ring chromosome 15
• Meiotic analysis of XX/XY and neo-XX/XY sex chromosomes in Phyllostomidae by cross-species chromosome painting revealing a common chromosome 15-XY rearrangement in Stenodermatinae
• Methylation status of hypothalamic <em>Mkrn3</em> promoter across puberty
• Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalities
• Molecular characterization and evaluation of complex rearrangements in a case of ring chromosome 15
• Molecular characterization of a ring chromosome 15 in a fetus with intra uterine growth retardation and diaphragmatic hernia
• Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes
• Molecular cytogenetic characterization of ring chromosome 15 in three unrelated patients
• Molecular cytogenetic studies of children with marker chromosomes
• Molecular cytogenetic study of a case with ring chromosome 15
• Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients
• Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literature
• New causes of central precocious puberty: the role of genetic factors
• Ophthalmic treatment and vision care of a patient with rare ring chromosome 15: a case report
• Phenotypic delineation of ring chromosome 15 and Russell-Silver syndromes
• Prenatal diagnosis of a fetus with ring chromosomal 15 by two- and three-dimensional ultrasonography
• Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH
• Prenatal diagnosis of mosaic ring chromosome 15 with abnormal maternal serum Down syndrome screening and Dandy-Walker malformation
• Prenatal Sonographic Features of Ring Chromosome 15: A Case Report and Literature Review
• Psychological findings in three children with ring 15 chromosome
• Response to growth hormone therapy in ring chromosome 15: Review and evidence from a new case on possible beneficial effect in neurodevelopment
• Ring Chromosome 10 in a Case of Acute Promyelocytic Leukemia
• Ring chromosome 12 resulting from nonrandom telomeric associations with the short arm of chromosome 15 in a cerebellar astrocytoma
• Ring chromosome 15 - cytogenetics and mapping arrays: a case report and review of the literature
• Ring chromosome 15 and 15qs+ mosaic: clinical and cytogenetic behaviour spanning 29 years
• Ring chromosome 15 in a mother and her children
• Ring chromosome 15 in a patient with features of Fryns' syndrome
• Ring chromosome 15 involving deletion of the insulin-like growth factor 1 receptor gene in a patient with features of Silver-Russell syndrome
• Ring chromosome 15 syndrome in an adult female
• Ring chromosome 15 syndrome. Further delineation of the adult phenotype
• Ring chromosome 15: characterization by array CGH
• Ring chromosome 15: expanding the phenotype
• Ring chromosome 15: follow-up data on physical and psychological development
• Ring chromosome 6 and i(17q-) in a patient with acute promyelocytic leukemia. Absence of translocation t(15;17)
• Ring syndrome: still true?
• Severe growth failure associated with atrophic intestinal mucosa and ring chromosome 15
• Small supernumerary marker chromosome 15 and a ring chromosome 15 associated with a 15q26.3 deletion excluding the IGF1R gene
• Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectives
• Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridization
• The identification of small supernumerary marker chromosomes; the experiences of 15,792 fetal karyotyping from Turkey
• The mouse and human genes encoding the recognition component of the N-end rule pathway
• The normality of sperm in an infertile man with ring chromosome 15: a case report
• The phenotype and rhGH treatment response of ring Chromosome 15 Syndrome: Case report and literature review
• The t(15;17) translocation in acute promyelocytic leukemia
• Trisomy and tetrasomy 15q11-q13 diagnosed by molecular cytogenetic analysis in two patients with mental retardation
• Trisomy of medial 15q as result of an analphoid supernumerary ring chromosome detected by CGH and FISH
• Twenty-year cytogenetic and molecular follow-up of a patient with ring chromosome 15: a case report
• Two new cases of analphoid marker chromosomes
• Two patients with ring chromosome 15 syndrome
• Unmasking 15q12 deletion using microarray-based comparative genomic hybridization in a mentally retarded boy with r(Y)