• 18q22.3 --> 18q23 deletion syndrome and cleft palate
• A boy with partial dup(18q)/del(18p) due to a maternal pericentric inversion: Genotype-phenotype correlation and risk of recombinant chromosomes based on systematic review of the literature
• A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review
• A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region
• A new deletion of 18q23 with few typical features of the 18q- syndrome
• A phenotypically diverse family with an atypical 22q11.2 deletion due to an unbalanced 18q23;22q11.2 translocation
• Abnormal brain MRI signal in 18q-syndrome not due to dysmyelination
• Abnormal myelination in ring chromosome 18 syndrome
• Allelic analysis of serous ovarian carcinoma reveals two putative tumor suppressor loci at 18q22-q23 distal to SMAD4, SMAD2, and DCC
• An Idic(7)(q11.2) Resulting in Two Copies of 7p and Deletion 7q: A Rare Cytogenetic Event in a Case of Acute Myeloid Leukemia
• Anterior segment malformations in 18q- (de Grouchy) syndrome
• Autoimmune polyendocrinopathy associated with ring chromosome 18
• Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y
• Beckwith-Wiedemann-like macroglossia and 18q23 haploinsufficiency
• Chromosome 18q paracentric inversion in a family with mental retardation and hearing loss
• Clinical and Cytogenomic Characterization of De Novo 11p14.3-p15.5 Duplication Associated with 18q23 Deletion in an Egyptian Female Infant
• Cognitive ability predicts degree of genetic abnormality in participants with 18q deletions
• Congenital aural atresia in 18q deletion or de Grouchy syndrome
• Cytogenetic, Molecular, and Phenotypic Characterization of a Patient with de novo Derivative Chromosome 18 and Review of the Literature
• Definition of a critical region on chromosome 18 for congenital aural atresia by arrayCGH
• Delineation and candidate gene mutation screening of the 18q22 minimal region of deletion in head and neck squamous cell carcinoma
• Familial 4.8 MB deletion on 18q23 associated with growth hormone insufficiency and phenotypic variability
• Frequent loss of heterozygosity on chromosome arm 18q in squamous cell carcinomas. Identification of 2 regions of loss--18q11.1-q12.3 and 18q21.1-q23
• Genetic alterations of microsatellites on chromosome 18 in human breast carcinoma
• Global brain dysmyelination with above-average verbal skills in 18q- syndrome with a 17 Mb terminal deletion
• Growth hormone insufficiency associated with haploinsufficiency at 18q23
• Highly conserved non-coding sequences and the 18q critical region for short stature: a common mechanism of disease?
• Identification of 2.3-Mb gene locus for congenital aural atresia in 18q22.3 deletion: a case report analyzed by comparative genomic hybridization
• Identification of new minimally lost regions on 18q in head and neck squamous cell carcinoma
• Linkage analysis of families with bipolar illness and chromosome 18 markers
• Microdeletion 15q26.2qter and Microduplication 18q23 in a Patient with Prader-Willi-Like Syndrome: Clinical Findings
• Molecular characterization of a patient with central nervous system dysmyelination and cryptic unbalanced translocation between chromosomes 4q and 18q
• Molecular characterization of patients with 18q23 deletions
• Paroxysmal periodic dystonic postures in an infant with 18q23 deletion syndrome
• Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia
• Prenatal diagnosis and molecular cytogenetic characterization of an inherited microdeletion of 18q12.3 encompassing SETBP1
• SALL3, a new member of the human spalt-like gene family, maps to 18q23
• Sensorineural hearing loss in people with deletions of 18q: hearing in 18q-
• Sperm FISH analysis in two healthy infertile brothers with t(15;18) unbalanced translocation: Implications for genetic counselling and reproductive management
• The human cytochrome b5 gene and two of its pseudogenes are located on chromosomes 18q23, 14q31-32.1 and 20p11.2, respectively
• Unbalanced translocation, t(18;21), detected by fluorescence in situ hybridization (FISH) in a child with 18q- syndrome and a ring chromosome 21