• 15q overgrowth syndrome: a newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q
• 15q13.3 duplication in two patients with childhood-onset schizophrenia
• A 15q25.2 microdeletion phenotype for premature ovarian failure in a Chinese girl: a case report and review of literature
• A cytogenetic study of nonpolymalformed patients with mental retardation of clinically undefined etiology: application of a high resolution banding technique
• A FURTHER PATIENT OF PURE 15q DELETION: CLINICAL AND MOLECULAR CYTOGENETIC FINDINGS
• A large polymorphic repeat in the pericentromeric region of human chromosome 15q contains three partial gene duplications
• An emerging phenotype of interstitial 15q25.2 microdeletions: clinical report and review
• Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs
• Analysis of cytogenetic aberrations in esthesioneuroblastomas by comparative genomic hybridization
• Analysis of imprinted genes in subjects with Prader-Willi syndrome and chromosome 15 abnormalities
• Angelman Syndrome Caused by Chromosomal Rearrangements: A Case Report of 46,XX,+der(13)t(13;15)(q14.1;q12)mat,-15 with an Atypical Phenotype and Review of the Literature
• Apparent germline mosaicism for a 15q11-q13 deletion causing recurrent Angelman syndrome in a Chinese family
• AZFc region of the Y chromosome shows singular structural organization
• Cell proliferation activities on skin fibroblasts from a short child with absence of one copy of the type 1 insulin-like growth factor receptor (IGF1R) gene and a tall child with three copies of the IGF1R gene
• Characterization of a 520 kb deletion on chromosome 15q26.1 including ST8SIA2 in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy: additional information
• Characterization of nonrandom chromosomal gains and losses in multiple myeloma by comparative genomic hybridization
• Chromosomal abnormalities associated with neural tube defects (II): partial aneuploidy
• Chromosomal abnormalities associated with omphalocele
• Chromosomal rearrangements detected by FISH and G-banding
• Chromosome 15q BP4-BP5 Deletion in a Girl with Nocturnal Frontal Lobe Epilepsy, Migraine, Circumscribed Hypertrichosis, and Language Impairment
• Chromosome microarray analysis: a case report of infertile brothers with CATSPER gene deletion
• Clinical phenotype and genetic analysis of a patient with a heterozygous 6p25.3 deletion and partial trisomy 15q
• Compulsions in Prader-Willi syndrome: occurrence and severity as a function of genetic subtype
• Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q
• Congenital stationary night blindness in a patient with mild learning disability due to a compound heterozygous microdeletion of 15q13 and a missense mutation in <em>TRPM1</em>
• Copy number variations could predict the outcome of bortezomib plus melphalan and prednisone for initial treatment of multiple myeloma
• Craniosynostosis associated with partial duplication of 15q and deletion of 2q
• De novo unbalanced translocations in Prader-Willi and Angelman syndrome might be the reciprocal product of inv dup(15)s
• Decline of CSF orexin (hypocretin) levels in Prader-Willi syndrome
• Detection of an unexpected subtelomeric 15q26.2 --&gt; qter deletion in a little girl: clinical and cytogenetic studies
• Detection of mutually exclusive mosaicism in a girl with genotype-phenotype discrepancies
• Diagnosis of familial Wolf-Hirschhorn syndrome due to a paternal cryptic chromosomal rearrangement by conventional and molecular cytogenetic techniques
• Diagnosis of Prader-Willi syndrome. Considerations on a case of erroneous diagnosis
• Distal Partial Trisomy 15q26 and Partial Monosomy 16p13.3 in a 36-Year-Old Male with Clinical Features of Both Chromosomal Abnormalities
• Distal trisomy of 10q with distal monosomy of 15q due to a paternal translocation
• Early onset myoclonic epilepsy and 15q26 microdeletion: observation of the first case
• Effect of Genotype and Previous GH Treatment on Adiposity in Adults With Prader-Willi Syndrome
• Evidence that Griscelli syndrome with neurological involvement is caused by mutations in RAB27A, not MYO5A
• Familial partial trisomy 15q11-13 presenting as intractable epilepsy in the child and schizophrenia in the mother
• Happy Puppet syndrome
• High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy
• Isolated del(5q) in myeloid malignancies: clinicopathologic and molecular features in 143 consecutive patients
• Mantle cell lymphomas with clonal immunoglobulin V(H)3-21 gene rearrangements exhibit fewer genomic imbalances than mantle cell lymphomas utilizing other immunoglobulin V(H) genes
• Metabolic syndrome in adult patients with Prader-Willi syndrome
• Molecular study of the Prader-Willi syndrome: deletion, RFLP, and phenotype analyses of 50 patients
• Myoclonic epilepsy, neuroblast migration disorders, and maternally derived partial duplication 14q/deletion 15q
• Partial 5p Gain and 15q Loss in Three Patients from a Family with a t(5;15)(p13.3;q26.3) Translocation
• Partial cerebellar hypoplasia in a patient with Prader-Willi syndrome
• Partial monosomy 15q due to de novo t(15;22)(q15;p11)
• Partial monosomy of 10p and duplication of another chromosome in two patients
• Partial tetrasomy of the proximal long arm of chromosome 15 in two patients: the significance of the gene dosage in terms of phenotype
• Partial trisomy of chromosome 15
• Phenotype-genotype correlation of a patient with a "balanced" translocation 9;15 and cryptic 9q34 duplication and 15q21q25 deletion
• Polymerase chain reaction allelotyping of human ovarian cancer
• Postnatal overgrowth by 15q-trisomy and intrauterine growth retardation by 15q-monosomy due to familial translocation t(13;15): dosage effect of IGF1R?
• Prader-Willi syndrome in two siblings: one with normal karyotype, one with a terminal deletion of distal Xq
• Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection
• Prenatal Diagnosis of Combined Maternal 4q Interstitial Deletion and Paternal 15q Microduplication
• Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal
• Prenatal diagnosis of the Dandy-Walker malformation associated with partial trisomy 12p and distal 15q deletion
• Problem behaviors associated with deletion Prader-Willi, Smith-Magenis, and cri du chat syndromes
• Proximal and distal 15q25.2 microdeletions-genotype-phenotype delineation of two neurodevelopmental susceptibility loci
• Siblings with deletion 22q13.3 and trisomy 15q26 inherited from a maternally balanced translocation
• Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis
• Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities
• Terminal 2q deletion and partial trisomy chromosome 15q: a clinical and cytogenetic study
• The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder
• The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum
• Tumor suppressor loci on mouse chromosomes 9 and 16 are lost at distinct stages of tumorigenesis in a transgenic model of islet cell carcinoma
• U-type exchange is the most frequent mechanism for inverted duplication with terminal deletion rearrangements
• Williams Syndrome and 15q Duplication: Coincidence versus Association