Disease: Chromosome 10- distal trisomy 10q
- "Molecular rulers" for calibrating phenotypic effects of telomere imbalance
- A 3 1/2 year old girl with distal trisomy 19q defined by FISH
- A Patient with Trisomy 4p and Monosomy 10q
- Absence of correlation between late-replication and spreading of X inactivation in an X;autosome translocation
- Chromosomal 10Q26 trisomy resulting from paternal T(9;10)(PTER;Q26.1)
- Complex distal 10q rearrangement in a girl with mild intellectual disability: follow up of the patient and review of the literature of non-acrocentric satellited chromosomes
- De novo der(X)t(X;10)(q26;q21) with features of distal trisomy 10q: case report of paternal origin identified by late replication with BrdU and the human androgen receptor assay (HAR)
- Distal 10q trisomy associated with bilateral hydronephrosis in infancy
- Distal 10q trisomy syndrome with unusual cardiac and pulmonary abnormalities
- Distal 10q trisomy with copy number gain in chromosome region 10q23.1-10q25.1: the Wnt signaling pathway is the most pertinent to the gene content in the region of copy number gain: a case report
- Distal trisomy 10q and limb defects
- Distal trisomy 10q due to maternal insertional translocation (15;10): A case report and review of literature
- Distal trisomy 10q syndrome, report of a patient with duplicated q24.31 - qter, autism spectrum disorder and unusual features
- Distal trisomy 10q syndrome: phenotypic features in a child with inverted duplicated 10q25.1-q26.3
- Distal trisomy 10q/partial monosomy 14q: an unusual clinical picture
- Distal trisomy of 10q with distal monosomy of 15q due to a paternal translocation
- Distal trisomy of 10q. Report of a new case of duplication 10q25.2-25.3-->qter defined by FISH
- Extreme growth failure and kyphoscoliosis as complications of the distal trisomy 10q syndrome
- Familial 3-Way Balanced Translocation Causes 1q43→qter Loss and 10q25.2→qter Gain in a Severely Affected Male Toddler
- Familial complex 3q;10q rearrangement unraveled by subtelomeric FISH analysis
- Neonatal death in cousins with trisomy 10q and monosomy 4p due to a familial translocation
- Novel Unbalanced Translocations Affecting the Long Arms of Chromosomes 10 and 22 Cause Complex Syndromes with Very Severe Neurodevelopmental Delay, Speech Impairment, Autistic Behavior, and Epilepsy
- Partial distal 10q trisomy due to de novo amplification: A new case without furrows or ridges in fingers and palms
- Partial duplication of 3q and distal deletion of 10q inherited from a maternal balanced translocation
- Partial trisomy 10q in three unrelated patients
- Partial trisomy of the distal part of 10q: a report of two Egyptian cases
- 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 of a fetus with distal 10q trisomy
- Prenatal diagnosis of Cri-du-Chat syndrome with concomitant distal trisomy 10q syndrome in one fetus with ultrasound anomalies
- Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results
- Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature
- 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
- Sacrococcygeal teratoma in a fetus with prenatally diagnosed partial trisomy 10q (10q24.3-->qter) and partial monosomy 17p (p13.3-->pter)
- Severe musculoskeletal phenotype associated with an unbalanced t(6;10) translocation: clarification of the locus for this phenotype on distal 6p
- Trisomy 10p syndrome owing to maternal pericentric inversion
- Trisomy 10qter confirmed by in situ hybridisation
- Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation