Disease: Chromosome 14q- partial deletions
- 14q32 deletion syndrome: a clinical report
- 18p--syndrome resulting from 14q/18q 'dicentric' fusion translocation
- A case of partial 14q- with facial features of holoprosencephaly and hydranencephaly
- A case with partial trisomy 7 (q34→qter) derived from a paternal reciprocal translocation t(7;14)(q34;q32)
- A molecular portrait of gastrointestinal stromal tumors: an integrative analysis of gene expression profiling and high-resolution genomic copy number
- A phenotype map for 14q32.3 terminal deletions
- A terminal deletion (14)(q31.1) in a child with microcephaly, narrow palate, gingival hypertrophy, protuberant ears, and mild mental retardation
- Acute lymphocytic leukemia with 9p anomalies. A report of four additional cases and review of the literature
- Adult T-cell leukemia. Chromosome analysis of 15 cases
- An analysis of chromosome findings in non-Hodgkin's lymphomas
- Chromosomal aberrations in chordoid meningioma - An analysis
- Chromosomal abnormalities associated with neural tube defects (II): partial aneuploidy
- Chromosome analyses of 16 cases of Wilms tumor: different pattern in unfavorable histology
- Copy number variations could predict the outcome of bortezomib plus melphalan and prednisone for initial treatment of multiple myeloma
- Cytogenetic abnormalities in tumors of patients with von Hippel-Lindau disease
- Cytogenetic studies and clinical aspects of patients with plasma cell leukemia and leukemic macroglobulinemia
- De novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1 → pter) and 14q (14q32.31 → qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction, and single umbilical artery: prenatal diagnosis and molecular
- De novo unbalanced translocation resulting in monosomy for proximal 14q and distal 4p in a fetus with intrauterine growth retardation, Wolf-Hirschhorn syndrome, hypertrophic cardiomyopathy, and partial hemihypoplasia
- Deletion mapping of two potential chromosome 14 tumor suppressor gene loci in ovarian carcinoma
- Deletions at 14q in malignant mesothelioma detected by microsatellite marker analysis
- Distal trisomy 10q/partial monosomy 14q: an unusual clinical picture
- Distal trisomy 14q caused by a paternal translocation (6;14)
- DNA methylation and allelic losses on chromosome arm 14q in oligodendroglial tumours
- Genetic abnormalities in chronic lymphocytic leukemia and their clinical and prognostic implications
- Genetic heterogeneity of neuroblastoma studied by comparative genomic hybridization
- Genomic study in patients with idiopathic azoospermia and oligoasthenoteratozoospermia
- Inherited 14q duplication and 21q deletion: a rare adjacent-2 segregation in multiple family members
- Interstitial deletion 14q31.1q31.3 transmitted from a mother to her daughter, both with features of hemifacial microsomia
- Interstitial deletion of 14q24.3-q32.2 in a male patient with plagiocephaly, BPES features, developmental delay, and congenital heart defects
- Loss of heterozygosity of chromosome 14q in low- and high-grade meningiomas
- Loss of heterozygosity on chromosome 14 in nasopharyngeal carcinoma
- Lymph node hyperplasia: clonal chromosomal and genomic rearrangements. Report of two new cases and literature review
- Lymphoblastic lymphoma: cytogenetic, pathologic, and immunologic studies
- Molecular cytogenetic definition of three distinct chromosome arm 14q deletion intervals in gastrointestinal stromal tumors
- Mosaic monosomy 14: clinical features and recognizable facies
- Multicentre analysis of patterns of DNA gains and losses in 204 neuroblastoma tumors: how many genetic subgroups are there?
- Multiple DICER1-related tumors in a child with a large interstitial 14q32 deletion
- Myoclonic epilepsy, neuroblast migration disorders, and maternally derived partial duplication 14q/deletion 15q
- Novel 14q11.2 microduplication including the CHD8 and SUPT16H genes associated with developmental delay
- Novel recurrent chromosomal aberrations detected in clonal plasma cells of light chain amyloidosis patients show potential adverse prognostic effect: first results from a genome-wide copy number array analysis
- Novel suppressor loci on chromosome 14q in primary bladder cancer
- Ophthalmic and systemic findings in interstitial deletions of chromosome 14q: a case report and literature review
- Partial allelotype of carcinoma in situ of the human bladder
- Partial deletion of 14q and partial duplication of 14q in sibs: testicular mosaicism for t(14q;14q) as a common mechanism
- Partial duplication 14q/deletion 2q in two sibs due to t(2;14) (q37.1;q31.2) pat
- Partial monosomy 7q
- Partial trisomy 14q
- Polymerase chain reaction allelotyping of human ovarian cancer
- Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication
- Prenatal diagnosis of partial trisomy 14q (14q31.1-->qter) and partial monosomy 5p (5p13.2-->pter) associated with polyhydramnios, short limbs, micropenis and brain malformations
- Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints
- Striking facial dysmorphisms and restricted thymic development in a fetus with a 6-megabase deletion of chromosome 14q
- The proximal chromosome 14q microdeletion syndrome: delineation of the phenotype using high resolution SNP oligonucleotide microarray analysis (SOMA) and review of the literature
- Two cases of partial trisomy 21 (pter-q22.1) without the major features of Down syndrome
- Unbalanced 14;X Translocation and Pattern of X Inactivation in a Female Patient with Multiple Congenital Anomalies
- Unbalanced cryptic translocation der(14)t(9;14)(q34.3;q32.33) identified by subtelomeric FISH