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One or more keywords matched the following items that are connected to Mulvihill, John
Item TypeName
Concept Chromosome Aberrations
Concept Chromosome Banding
Concept Chromosome Deletion
Concept Chromosome Fragility
Concept Chromosome Mapping
Concept Chromosomes, Human, Pair 1
Concept Chromosomes, Human, Pair 10
Concept Chromosomes, Human, Pair 11
Concept Chromosomes, Human, Pair 14
Concept Chromosomes, Human, Pair 15
Concept Chromosomes, Human, Pair 17
Concept Chromosomes, Human, Pair 18
Concept Chromosomes, Human, Pair 2
Concept Chromosomes, Human, Pair 21
Concept Chromosomes, Human, Pair 22
Concept Chromosomes, Human, Pair 4
Concept Chromosomes, Human, Pair 5
Concept Chromosomes, Human, Pair 6
Concept Chromosomes, Human, Pair 8
Concept Chromosomes, Human, Pair 9
Concept Chromosome Inversion
Concept Sex Chromosome Aberrations
Concept X Chromosome
Concept Chromosome Disorders
Concept Chromosome Duplication
Academic Article Inheritance of pancreatic cancer in pancreatic cancer-prone families.
Academic Article Duplication 15q in a patient with t(8;21) acute myeloblastic leukemia (M2).
Academic Article Rapid prenatal diagnosis of trisomies 13, 18, 21 and sex chromosome anomalies by fluorescence in situ hybridization: a year's experience.
Academic Article Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
Academic Article A novel subtelomeric translocation t(5;9) and a deletion of the RB1 gene in a patient with acute myeloid leukemia (AML-M0).
Academic Article Statement on bioinformatics and capturing the benefits of genome sequencing for society.
Academic Article Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1).
Academic Article Multipoint linkage analysis in neurofibromatosis type I: an international collaboration.
Academic Article Sister chromatid exchange and chromosome fragility in the nevoid basal cell carcinoma syndrome.
Academic Article Caffeine as teratogen and mutagen.
Academic Article Localization of the gene for Cowden disease to chromosome 10q22-23.
Academic Article Familial eosinophilia: clinical and laboratory results on a U.S. kindred.
Academic Article Double trisomy.
Academic Article Ring chromosome 9 [r(9)(p24q34)]: a report of two cases.
Academic Article Reversed clinical phenotype due to a microduplication of Sotos syndrome region detected by array CGH: microcephaly, developmental delay and delayed bone age.
Academic Article High-resolution analysis of copy number variants in adults with simple-to-moderate congenital heart disease.
Academic Article Evidence of genetic heterogeneity in five kindreds with familial hypertrophic cardiomyopathy.
Academic Article Genetic linkage analysis of neurofibromatosis.
Academic Article Fatal hypereosinophilia with chromosome 15q- in a patient with multiple primary and familial neoplasms.
Academic Article International Commission for Protection against Environmental Mutagens and Carcinogens. ICPEMC Working Paper 5/6. Perspectives in mutation epidemiology, 6. A 1983 view of sentinel phenotypes.
Academic Article Neurofibromatosis: no chromosomal defect by prophase banding technique.
Academic Article Patterns of inheritance in hypertrophic cardiomyopathy: assessment by M-mode and two-dimensional echocardiography.
Academic Article Chromosome 2q terminal deletion: report of 6 new patients and review of phenotype-breakpoint correlations in 66 individuals.
Academic Article A variant t(8;10;21) in a patient with pathological features mimicking atypical chronic myeloid leukemia.
Academic Article Cytogenetic and molecular cytogenetic studies of a variant of t(21;22), ins(22;21)(q12;q21q22), with a deletion of the 3' EWSR1 gene in a patient with Ewing sarcoma.
Academic Article Automated identification of abnormal metaphase chromosome cells for the detection of chronic myeloid leukemia using microscopic images.
Academic Article Genetic disease in the children of Danish survivors of childhood and adolescent cancer.
Academic Article A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome.
Academic Article Duplication 15q as the sole anomaly in an acute promyelocytic leukemia patient without t(15;17).
Academic Article Identification of t(15;17) and a segmental duplication of chromosome 11q23 in a patient with acute myeloblastic leukemia M2.
Academic Article Leiomyosarcoma of the breast: a pathologic and comparative genomic hybridization study of two cases.
Academic Article Chromosomal abnormalities among offspring of childhood-cancer survivors in Denmark: a population-based study.
Academic Article A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome.
Academic Article Down syndrome with pure partial trisomy 21q22 due to a paternal insertion (4;21) uncovered by uncultured amniotic fluid interphase FISH.
Academic Article Ring chromosome 4 in a patient with early onset type 2 diabetes, deafness, and developmental delay.
Academic Article Trisomy 1q in a patient with severe aplastic anemia.
Academic Article De novo three-way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia.
Academic Article Deletion of 14q24.1 approximately q24.3 in a patient with acute lymphoblastic leukemia: a hidden chromosomal anomaly detected by array-based comparative genomic hybridization.
Academic Article Chromosomal Abnormalities in Offspring of Young Cancer Survivors: A Population-Based Cohort Study in Denmark.
Academic Article Multiple childhood osteosarcomas in an American Indian family with erythroid macrocytosis and skeletal anomalies.
Academic Article Genetics of SV40 T-antigen expression: studies of twins, heritable syndromes and cancer families.
Academic Article Cytogenetics in hereditary malignant melanoma and dysplastic nevus syndrome: is dysplastic nevus syndrome a chromosome instability disorder?
Search Criteria
  • Chromosomes Human Pair 1