• 'Pure' partial trisomy 4q26-->q35.2 resulting from a familial unbalanced translocation t(4;10)(q26;q26.3)
• 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes
• 46,XX/46,XX,del (10) (p13)/47,XX,+r/47,XX,del (10) (p13), + r mosaicism and partial trisomy 10p phenotype (author's transl)
• A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review
• A fetus with trisomy 9p and trisomy 10p originating from unbalanced segregation of a maternal complex chromosome rearrangement t(4;10;9)
• A novel dic(1;10) in a patient with myelodysplastic syndrome
• A novel unbalanced whole-arm translocation der(3;10)(q10;q10) in acute monocytic leukemia
• A Unique Genomic Variant of HDR Syndrome in Newborn
• Brother and sister with trisomy 10p. 46,XY,(22p+)mat; 46,XX,(22p+)mat
• Characterization of familial partial 10p trisomy by chromosomal microdissection, FISH, and microsatellite dosage analysis
• Chromosome 10p11.2-p12.2 duplication: report of a patient and review of the literature
• Combined 10pter-->p11 and 18pter-->q11 trisomy in a 7-year-old child
• Combined partial trisomy 11q and partial monosomy 10p in a 19-year-old female patient: phenotypic and genotypic findings
• Complete trisomy 10p resulting from an extra stable telocentric chromosome
• DiGeorge syndrome and partial monosomy 10p: case report and review
• Duplication deficiency as the result of meiotic segregation of a maternal InV (10)
• Early urethral obstruction sequence and unbalanced translocation with terminal 10p duplication/1p deficiency
• Familial 10p trisomy resulting from a maternal pericentric inversion
• Family with partial monosomy 10p and trisomy 10p
• Identification and characterization of a de novo partial trisomy 10p by comparative genomic hybridization (CGH)
• Increased HK1 activity levels in the red cells of a patient with a de novo trisomy 10p: t(Y;10)(p11;p12)
• Kabuki syndrome and trisomy 10p
• Molecular cytogenetics, RFLP analysis and clinical characterization of a de novo trisomy 10p case
• Multiorgan autoimmunity in a Turner syndrome patient with partial monosomy 2q and trisomy 10p
• Myeloid Antigen-positive T Cell Acute Lymphocytic Leukemia with t(14;18) and Trisomy 10: Report of a Case and Literature Review
• Neonatal pancytopenia associated with de novo 1q43-44 deletion and 10p15 duplication
• Neurophysiological findings in a newborn with chromosome 10 trisomy
• New chromosomal dysmorphic syndromes. 2. Trisomy 10p
• Oligo-elements of the amniotic fluid from normal, hypotrophic and trisomy 21 fetuses
• Ophthalmic findings in partial monosomy 4p (Wolf syndrome) in combination with partial trisomy 10p
• Partial duplication of the short arm of chromosome 10. Karyotype: 46,XX,dup(10p)(pter to p12::p12::p12 to qter)
• Partial monosomy of 10p and duplication of another chromosome in two patients
• Partial trisomy 10 mosaicism with cutaneous manifestations: report of a case and review of the literature
• Partial trisomy 10p
• Partial trisomy 10p and familial translocation t(7;10)(p22;p12)
• Partial trisomy 10p in combination with partial monosomy 20p--a syndrome with muscular hypotonia, psychomotor retardation, dwarfism and craniofacial dysmorphia
• Partial trisomy 10p12.33 and partial monosomy 13q32.1: case report and a literature review
• Phenotypic and genetic analysis of a boy with a 10p15.3 deletion and partial trisomy 18p syndrome
• Prenatal detection of a pure trisomy 10p case
• Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion
• Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literature
• Pure trisomy 10p involving an isochromosome 10p
• Pure trisomy 10p resulting from an extra ring chromosome: characterization by methods of advanced molecular cytogenetics
• Regional localization of the gene coding for sphingolipid activator protein SAP-1 on human chromosome 10
• Regional mapping of hexokinase-1 within the short arm of chromosome 10
• Relatives with opposite chromosome constitutions, rec(10)dup(10p)inv(10)(p15.1q26.12) and rec(10)dup(10q)inv(10)(p15.1q26.12), due to a familial pericentric inversion
• Risk for short arm 10 trisomy. A segregation analysis of eleven families with different translocations
• Simultaneous partial monosomy 10p and trisomy 5q in a case of hypoparathyroidism
• Small supernumerary marker chromosome originating from chromosome 10 associated with an apparently normal phenotype
• Subtelomeric 6.7 Mb trisomy 10p and 5.6 Mb monosomy 21q detected by FISH and array-CGH in three related patients
• Subtelomeric analysis detects a familial 10p;12p rearrangement in two relatives with a distinct syndrome
• The dermatoglyphic pattern of the trisomy 10p syndrome
• Trisomy 10p and translocation of 10q to 4p associated with selective dysgenesis of IgA-producing cells in lymphoid tissue
• Trisomy 10p produced by recombination involving maternal inversion inv(10)(pllq26)
• Trisomy 10p syndrome owing to maternal pericentric inversion
• Trisomy 10p with clinical features of facio-auriculo-vertebral spectrum: a case report
• Trisomy 10p: report of an unusual mechanism of formation and critical evaluation of the clinical phenotype
• Trisomy for the short arm of chromosome 10. Report of a new case resulting from segregation of a maternal balanced translocation t(10qter----q11::14p11----qter)
• Trisomy of the short arm of chromosome 10
• Trisomy of the short arm of chromosome 10p; description of a female patient with de novo duplication 10p11.2-15
• Two chromosomal syndromes in the same family: monosomy and trisomy for part of the short arm of chromosome 10
• Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion