• 'Pure' partial trisomy 4q26-->q35.2 resulting from a familial unbalanced translocation t(4;10)(q26;q26.3)
• 10p monosomy, a phenotypic variant
• 10p- syndrome associated with multiple chromosomal abnormalities
• 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 case of 10p- syndrome
• A case of de novo translocation 7; 10 and the duplication 7p, deletion 10p phenotype
• A case of deletion of the short arm of chromosome 10 with severe hearing loss and brainstem dysfunction
• A common region of 10p deleted in DiGeorge and velocardiofacial syndromes
• A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability
• A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review
• 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 patient with apparently reciprocal translocation and cryptic 10p deletion
• Allelic loss of chromosomes 16q and 10q in human prostate cancer
• Allelotyping of human prostatic adenocarcinoma
• An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus maps distal to the DiGeorge syndrome region on 10p13/14
• Chromosome 10 deletion mapping in human gliomas: a common deletion region in 10q25
• Chromosome 10p deletion in a patient with hypoparathyroidism, severe mental retardation, autism and basal ganglia calcifications
• Combined partial trisomy 11q and partial monosomy 10p in a 19-year-old female patient: phenotypic and genotypic findings
• Congenital monoblastic leukemia cutis. A case report with chromosomal abnormality: del (10p)
• De novo partial monosomy 10p
• Deficiency 10p. Report of a case and exclusion mapping of the hexokinase 1 locus to band 10p11.2
• Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion
• Deletion of the short arm of chromosome 10 (10p13): report of a patient and review
• DiGeorge anomaly and chromosome 10p deletions: one or two loci?
• DiGeorge anomaly associated with 10p deletion
• DiGeorge syndrome and partial monosomy 10p: case report and review
• DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion
• Dinucleotide repeat polymorphisms at nine loci in sporadic colorectal cancer
• Distinct patterns of deletion on 10p and 10q suggest involvement of multiple tumor suppressor genes in the development of astrocytic gliomas of different malignancy grades
• Double partial monosomies (10p- and Xp-) in a female baby with choanal atresia
• Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci
• Early pediatric palliative care involvement in a child with a large deletion of the short arm (p) of chromosome 10: a case report
• Early urethral obstruction sequence and unbalanced translocation with terminal 10p duplication/1p deficiency
• Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p
• Familial 10p trisomy resulting from a maternal pericentric inversion
• Family with partial monosomy 10p and trisomy 10p
• Fine mapping of a region of common deletion on chromosome arm 10p in human glioma
• Fine-mapping subtelomeric deletions and duplications by comparative genomic hybridization in 42 individuals
• Frequent loss of heterozygosity on chromosome 10q in muscle-invasive transitional cell carcinomas of the bladder
• Gene amplification of atypical PKC-binding PARD3 in radiation-transformed neoplastic retinal pigment epithelial cell lines
• Genomic changes in primary lesion and lymph node metastases of esophageal squamous cell carcinoma
• Hypocalcemia impacts heart failure control in DiGeorge 2 syndrome
• Hypoparathyroidism with partial monosomy 10p
• Interstitial 10p deletion derived from a maternal ins(16;10)(q22;p13p15.2): Report of the first familial case of 10p monosomy affecting to two familial members of different generations
• Interstitial 10p11.23-p12.1 microdeletions associated with developmental delay, craniofacial abnormalities, and cryptorchidism
• Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndrome
• Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization
• Investigation of genetic alterations associated with the grade of astrocytic tumor by comparative genomic hybridization
• Juvenile polyposis of infancy associated with paracentric inversion and deletion of chromosome 10 in a Hispanic patient: a case report
• KLF6 is not the major target of chromosome 10p losses in glioblastomas
• Liver metastatic ability of human melanoma cell line is associated with losses of chromosomes 4, 9p21-pter and 10p
• Loss of 10p material in a child with human papillomavirus-positive disseminated bilateral retinoblastoma
• Loss of a small region around the PTEN locus is a major chromosome 10 alteration in prostate cancer xenografts and cell lines
• Loss of heterozygosity for alleles on chromosome 10 in human brain tumours
• Loss of heterozygosity of chromosome 10p in human gliomas
• Loss of heterozygosity of the retinoblastoma and adenomatous polyposis susceptibility gene loci and in chromosomes 10p, 10q and 16q in human prostate cancer
• Loss of heterozygosity on chromosomes 10 and 17 in clinically localized prostate carcinoma
• Mapping susceptibility gene locus for IgA deficiency at del(18)(q22.3-q23); report of familial cryptic chromosome t(18q; 10p) translocations
• Microsatellite instabilities at five chromosomes in primary breast tumors
• Molecular and clinical characterization of patients with overlapping 10p deletions
• Molecular cytogenetic characterization of a 10p14 deletion that includes the DGS2 region in a patient with multiple anomalies
• MRI findings in a patient with partial monosomy 10p
• Multiorgan autoimmunity in a Turner syndrome patient with partial monosomy 2q and trisomy 10p
• Neonatal pancytopenia associated with de novo 1q43-44 deletion and 10p15 duplication
• No evidence for chromosomal microdeletions at the second DiGeorge syndrome locus on 10p near D10S585
• Ophthalmic findings in partial monosomy 4p (Wolf syndrome) in combination with partial trisomy 10p
• Partial deletion 10p syndrome. Report of two patients
• Partial DiGeorge anomaly associated with 10p deletion
• Partial monosomy 10p in a case investigated with tomodensitometry (author's transl)
• Partial monosomy 10p syndrome
• Partial monosomy of 10p and duplication of another chromosome in two patients
• 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
• Pathways leading to glioblastoma multiforme: a molecular analysis of genetic alterations in 65 astrocytic tumors
• Phenotype comparison confirms ZMYND11 as a critical gene for 10p15.3 microdeletion syndrome
• Phenotypic and Brain Imaging Findings Associated With a 10p Proximal Deletion Including the WAC Gene: Case Report and Literature Review
• Phenotypic and genetic analysis of a boy with a 10p15.3 deletion and partial trisomy 18p syndrome
• 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
• Progressive deficiencies in blood T cells associated with a 10p12-13 interstitial deletion
• Pseudoarthrosis of the clavicle and copper beaten skull associated with chromosome 10p11.21p12.1 microdeletion
• Simultaneous partial monosomy 10p and trisomy 5q in a case of hypoparathyroidism
• 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
• Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features
• Subtelomeric fish findings in Turkish patients with idiopathic mental retardation
• T cell immunodeficiency in a patient with 10p deletion syndrome
• The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndrome
• 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