Disease: Chromosome 7- partial monosomy 7p
- 4q27 deletion and 7q36.1 microduplication in a patient with multiple malformations and hearing loss: a case report
- 7p deletion syndrome: an adult with mild manifestations
- 7p-deletion syndrome
- A case of de novo translocation 7; 10 and the duplication 7p, deletion 10p phenotype
- A FEMALE PATIENT WITH DUPLICATION OF 7p13-pter ASSOCIATED WITH DEL 20p13pter RESULTING FROM MALSEGREGATED PATERNAL 7;20 BALANCED TRANSLOCATION
- A fetus with an abnormal chromosome 7 and possible hydrolethalus syndrome
- A malformed child with a recombinant chromosome 7, rec(7) dup p, derived from a maternal pericentric inversion inv(7)(p15q36)
- A new dic(7;12)(p12.21;p12.2) chromosome aberration in a case of acute myeloid leukemia
- A novel syndrome of cerebral cavernous malformation and Greig cephalopolysyndactyly. Laboratory investigation
- A patient with duplication (7)(p15.3p22.3) and deletion (7)(p22.3pter) characterized by array-CGH
- A report of a patient with duplication of 7p13-->pter and deletion of 2p23-->pter due to a maternal 2p;7p translocation
- A report of a patient with duplication of 7p13-->pter and deletion of 2p23-->pter due to a maternal 2p;7p translocation
- A somatic cell hybrid panel and DNA probes for physical mapping of human chromosome 7p
- Acute lymphoblastic leukemia in a patient with Greig cephalopolysyndactyly and interstitial deletion of chromosome 7 del(7)(p11.2 p14) involving the GLI3 and ZNFN1A1 genes
- Acute myeloid leukemia with t(7;21)(p22;q22) and 5q deletion: a case report and literature review
- An Idic(7)(q11.2) Resulting in Two Copies of 7p and Deletion 7q: A Rare Cytogenetic Event in a Case of Acute Myeloid Leukemia
- Breakpoint-specific multiplex polymerase chain reaction allows the detection of IKZF1 intragenic deletions and minimal residual disease monitoring in B-cell precursor acute lymphoblastic leukemia
- Cardiac malformation of partial trisomy 7p/monosomy 18p and partial trisomy 18p/monosomy 7p in siblings as a result of reciprocal unbalanced malsegregation--and review of the literature
- Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay-Does both possibly act to modulate a candidate gene region for the patient's phenotype?
- CD34 expression is associated with major adverse prognostic factors in adult acute lymphoblastic leukemia
- Central neurocytomas are genetically distinct from oligodendrogliomas and neuroblastomas
- Characterization of aneuploid populations with trisomy 7 and 20 derived from diploid human colonic epithelial cells
- Characterization of deletions of chromosome 7 short arm occurring as primary karyotypic anomaly in acute myeloid leukaemia
- Characterization of human laryngeal primary and metastatic squamous cell carcinoma cell lines UM-SCC-17A and UM-SCC-17B
- Chromosome 7 aberrations in a young girl with myelodysplasia and hepatoblastoma: an unusual association
- Chromosome 7p--syndrome: craniosynostosis with preservation of region 7p2
- Chromosome 7q deletions: observations on 13 malignant tumors
- Chromosome analyses of 16 cases of Wilms tumor: different pattern in unfavorable histology
- Clinical significance of isolated del(7p) in myeloid neoplasms
- Clonal chromosome abnormalities in 54 cases of ovarian carcinoma
- Comparative genomic hybridization of esophageal and gastroesophageal adenocarcinomas shows consensus areas of DNA gain and loss
- Comparative genomic hybridization reveals a specific pattern of chromosomal gains and losses during the genesis of colorectal tumors
- Complex balanced translocation t(1;5;7)(p32.1;q14.3;p21.3) and two microdeletions del(1)(p31.1p31.1) and del(7)(p14.1p14.1) in a patient with features of Greig cephalopolysyndactyly and mental retardation
- Cytogenetic analysis of 63 non-small cell lung carcinomas: recurrent chromosome alterations amid frequent and widespread genomic upheaval
- Cytogenetic and molecular analysis of an unbalanced translocation (X;7) (q28;p15) in a dysmorphic girl
- Deletion 7p in gastric MALT lymphoma
- Deletion of (7p13p14) in non-Hodgkin's lymphoma
- Deletion of 7p or monosomy 7 in pediatric acute lymphoblastic leukemia is an adverse prognostic factor: a report from the Children's Cancer Group
- Deletion of 7p: lymphoid and non-lymphoid disorders cluster in different break points
- Deletions of chromosome arms 7p and 7q in adult acute myeloid leukemia: a marker chromosome confirmed by array comparative genomic hybridization
- Delineation of a less than 200 kb minimal deleted region for cardiac malformations on chromosome 7p22
- Demonstration of acquired hemizygosity and clonality in acute lymphoblastic leukemia with chromosome 7 abnormalities using hypervariable DNA probes
- Detailed analysis of clonal evolution and cytogenetic evolution patterns in patients with myelodysplastic syndromes (MDS) and related myeloid disorders
- Discordant phenotypes in a mother and daughter with mosaic supernumerary ring chromosome 19 explained by a de novo 7q36.2 deletion and 7p22.1 duplication
- Establishment and characterization of a new human acute myelomonocytic leukemia cell line JIH-3
- Evidence that the Saethre-Chotzen syndrome locus lies between D7S664 and D7S507, by genetic analysis and detection of a microdeletion in a patient
- Fluorescence in situ hybridization analysis of whole-arm 7;12 translocations in hematologic malignancies
- Frequent loss of heterozygosity on chromosomes 7 and 9 in benign epithelial ovarian tumours
- Genetic characterization of adult infratentorial gliomas
- Genomic alterations in low-grade, anaplastic astrocytomas and glioblastomas
- Genomic analysis of five chromosome 7p deletion patients with Greig cephalopolysyndactyly syndrome (GCPS)
- Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review
- Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13
- Hepatosplenic gammadelta T-cell lymphoma with ring chromosome 7, an isochromosome 7q equivalent clonal chromosomal aberration
- IKZF1 Deletions with COBL Breakpoints Are Not Driven by RAG-Mediated Recombination Events in Acute Lymphoblastic Leukemia
- Increased number of chromosomal imbalances and high-level DNA amplifications in mantle cell lymphoma are associated with blastoid variants
- Investigation of genetic alterations associated with the grade of astrocytic tumor by comparative genomic hybridization
- Is loss of band 7p21 really critical for manifestation of craniosynostosis in 7p-?
- Localization of genes and anonymous DNA probes on the short arm of chromosome 7
- Loss of 1p and 7p in radiation-induced meningiomas identified by comparative genomic hybridization
- Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumour
- Mapping of a putative tumor suppressor locus to proximal 7p in Wilms tumors
- Microdeletion of chromosome 7P syndrome ocular manifestations
- Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: hemizygosity for PGAM2 and TCRG genes
- Molecular and cytogenetic characterization of 9p- abnormalities
- Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature
- Molecular Karyotyping of a Dysmorphic Girl from Saudi Arabia with CYP1B1-negative Primary Congenital Glaucoma
- Monosomy 7p in meningiomas: a rare constituent of tumor progression
- Mutation screening in 18 Caucasian families suggest the existence of other MODY genes
- Parallel mapping and simultaneous sequencing reveals deletions in BCAN and FAM83H associated with discrete inherited disorders in a domestic dog breed
- Partial trisomy 16q and partial monosomy 7p of a fetus derivated from paternal balanced translocation: A case report
- Partial trisomy 3p and monosomy 7p associated with tetralogy of Fallot and infantile seizure
- Partial trisomy and partial monosomy resulting from a reciprocal segregating in a large family
- Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patient
- Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patient
- Phenotype and micro-array characterization of duplication 11q22.1-q25 and review of the literature
- Postnatal onset of craniosynostosis in a case of Saethre-Chotzen syndrome
- Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly
- Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3pter) and partial monosomy 13q (13q33.3qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly
- Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly
- Prenatal diagnosis of partial monosomy 5p (5p15.1pter) and partial trisomy 7p (7p15.2pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly
- Presence of 1q gain and absence of 7p gain are new predictors of local or metastatic relapse in localized resectable neuroblastoma
- Rare monosomy 7 and deletion 7p at diagnosis of chronic myeloid leukemia in accelerated phase
- Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours
- Secondary cytogenetic aberrations in childhood Philadelphia chromosome positive acute lymphoblastic leukemia are nonrandom and may be associated with outcome
- Segmental Maternal UPD of Chromosome 7q in a Patient With Pendred and Silver Russell Syndromes-Like Features
- Sequential numerical changes of chromosomes 7 and 18 in diffuse-type stomach cancer cell lines: combined comparative genomic hybridization, fluorescence in situ hybridization, and ploidy analyses
- Six cases of 7p deletion: clinical, cytogenetic, and molecular studies
- Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter)
- Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter)
- Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter)
- Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter)
- Structural aberrations of chromosome 7 revealed by a combination of molecular cytogenetic techniques in myeloid malignancies
- Telomere-telomere (end to end) fusion of chromosomes 7 and 22 with an interstitial deletion of chromosome 7p11.2-->p15.1: phenotypic consequences and possible mechanisms
- Telomere-telomere (end to end) fusion of chromosomes 7 and 22 with an interstitial deletion of chromosome 7p11.2-->p15.1: phenotypic consequences and possible mechanisms
- The prognostic impact of loss of chromosome 7 material detected by fluorescence in situ hybridization (FISH) in myeloid malignancies
- Two candidate tumor suppressor genes, MEOX2 and SOSTDC1, identified in a 7p21 homozygous deletion region in a Wilms tumor
- Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis
- Variable developmental delays and characteristic facial features-A novel 7p22.3p22.2 microdeletion syndrome?
- Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16