Disease: Chromosome 10p terminal deletion syndrome
- 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
- A common region of 10p deleted in DiGeorge and velocardiofacial syndromes
- Chromosomal rearrangements detected by FISH and G-banding
- Chromosome 10p deletion in a patient with hypoparathyroidism, severe mental retardation, autism and basal ganglia calcifications
- Clinical report of a neonate carrying a large deletion in the 10p15.3p13 region and review of the literature
- Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2)
- DiGeorge anomaly and chromosome 10p deletions: one or two loci?
- Early urethral obstruction sequence and unbalanced translocation with terminal 10p duplication/1p deficiency
- GATA3 haplo-insufficiency causes human HDR syndrome
- Goyal-Naqvi Syndrome (Concurrent Trisomy 10p and Terminal 14q Deletion): A Review of the Literature
- Hypocalcemia impacts heart failure control in DiGeorge 2 syndrome
- 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
- Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization
- Molecular and clinical characterization of patients with overlapping 10p deletions
- Neonatal pancytopenia associated with de novo 1q43-44 deletion and 10p15 duplication
- Partial DiGeorge syndrome in two patients with a 10p rearrangement
- Partial monosomy of 10p and duplication of another chromosome in two patients
- Phenotype comparison confirms ZMYND11 as a critical gene for 10p15.3 microdeletion syndrome
- Syndromic autism: II. Genetic syndromes associated with autism
- 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