• <em>De Novo</em> Pure Trisomy 20p: Report of a Novel Case of a Marker Chromosome and Literature Review
• "De Novo" trisomy 20p with macroorchidism in a prepuberal boy
• 20 p duplication as a result of parental translocation: familial case report and a contribution to the clinical delineation of the syndrome
• A cascade of chromosomal aberrations in three generations: a fragile 16q, an extra fragment and a rearranged 20
• A case of partial trisomy 20p resulting from meiotic recombination of a maternal pericentric inversion
• A FEMALE PATIENT WITH DUPLICATION OF 7p13-pter ASSOCIATED WITH DEL 20p13pter RESULTING FROM MALSEGREGATED PATERNAL 7;20 BALANCED TRANSLOCATION
• A Unique Genomic Variant of HDR Syndrome in Newborn
• Alagille syndrome in a family with duplication 20p11
• Analysis of a whole arm translocation between chromosomes 18 and 20 using fluorescence in situ hybridization: detection of a break in the centromeric alpha-satellite sequences
• Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings
• Chromosome 20p inverted duplication deletion identified in a Thai female adult with mental retardation, obesity, chronic kidney disease and characteristic facial features
• Chromosome 20p Partial <em>De Novo</em> Duplication Identified in a Female Paediatric Patient with Characteristic Facial Dysmorphism and Behavioural Anomalies
• Combined immunodeficiency in a 3-year-old boy with 16p11.2 and 20p12.2-11.2 chromosomal duplications
• Cytogenomic characterization of an unexpected 17.6 Mb 9p deletion associated to a 14.8 Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotype
• De novo partial duplication of 3q and distal deletion of 20p in a 15-week abort us with omphalocele
• De Novo Pure Trisomy 20p: Report of a Novel Case of a Marker Chromosome and Literature Review
• De novo trisomy 20p characterized by array comparative genomic hybridization: report of a novel case and review of the literature
• De novo trisomy 20p of paternal origin
• Dissecting the phenotype of supernumerary marker chromosome 20 in a patient with syndromic Pierre Robin sequence: combinatorial effect of gene dosage and uniparental disomy
• Distal monosomy 18p/distal trisomy 20p--a recognizable facial phenotype?
• Duplication (20p) in association with thyroid carcinoma
• Duplication 20p identified via fluorescent in situ hybridization
• Familial trisomy 20p five cases and two carriers in three generations a review
• Fluorescence in situ hybridization (FISH) of a whole-arm translocation involving chromosomes 18 and 20 with alpha-satellite DNA probes: detection of a centromeric DNA break?
• Intrachromosomal insertion mimicking a pericentric inversion: molecular cytogenetic characterization of a three break rearrangement of chromosome 20
• Intracytoplasmic sperm injection pregnancy with trisomy 20p and monosomy 22q in a newborn resulting from a balanced paternal translocation
• Laparoscopic Hysterectomy and Bilateral Salpingectomy in a Patient with Microduplication Syndrome (20p13p12.1) and a Bicornuate Uterus: An Unreported Association
• Lissencephaly with der(17)t(17;20)(p13.3;p12.2)mat
• Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization
• Maternally inherited partial monosomy 9p (pter p24.1) and partial trisomy 20p (pter p12.1) characterized by microarray comparative genomic hybridization
• Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U-type exchange model
• Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH)
• Mosaic tetrasomy 20p associated with osteoporosis and recurrent fractures
• New candidate region for mirror hand movements: two patients with terminal 9p deletion and 20p duplication
• Partial trisomy 10p in combination with partial monosomy 20p--a syndrome with muscular hypotonia, psychomotor retardation, dwarfism and craniofacial dysmorphia
• Partial trisomy 20p derived from a t(18;20) translocation
• Partial trisomy 20p resulting from a recombination of a familial pericentric inversion
• Partial trisomy 20p resulting from recombination of a maternal pericentric inversion: case report of a prenatal diagnosis by chorionic villus sampling
• Partial trisomy 20p: familial occurrence
• Prenatal diagnosis and fetal pathology of partial trisomy 20P-monosomy 4P resulting from paternal translocation
• Prenatal diagnosis of a de novo trisomy 20p detected by noninvasive prenatal testing
• Pure trisomy 20p resulting from isochromosome formation and whole arm translocation
• Short report: Twins with 20p13 duplication. Case report and comprehensive literature review
• SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variation
• Supernumerary ring chromosome 20 characterized by fluorescence in situ hybridization
• Trisomy 20p
• Trisomy 20p derived from a maternal pericentric inversion and brachymesophalangy of the index finger
• Trisomy 20p due to a paternal reciprocal translocation
• Trisomy 20p due to balanced maternal translocation t(3;20)
• Trisomy 20p from maternal t(3;20) translocation
• Trisomy 20p from maternal translocation and anencephaly. Case report and genetic review
• Trisomy 20p resulting from inverted duplication and neocentromere formation
• Trisomy 20p: case report and genetic review
• Trisomy 20p/monosomy 18p associated with congenital bilateral perisylvian syndrome
• Two siblings with alternate unbalanced recombinants derived from a large cryptic maternal pericentric inversion of chromosome 20
• Unbalanced three-way chromosomal translocation leading to deletion 18q and duplication 20p