About: Frederick Hecht

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

genetics researcher

Attributes	Values
rdf:type	Item
description	эрдэмтэн (mn) genetics researcher (en)
rdfs:label	Frederick Hecht (ca) Frederick Hecht (en) Frederick Hecht (nl)
skos:prefLabel	Frederick Hecht (ca) Frederick Hecht (en) Frederick Hecht (nl)
name	Frederick Hecht (ca) Frederick Hecht (en) Frederick Hecht (nl)
ResearchGate contributions ID	wds:Q100952417-9b09ca65-475d-95c9-9745-f5d0808cb1f4
ResearchGate contributions ID	39357725
Scopus author ID	wds:Q100952417-1845b821-4f6f-71de-20e4-f089fe638de8
Scopus author ID	57203105722
given name	wds:Q100952417-7ceace61-46fa-cd73-a0b6-958c6d07d96d
given name	Frederick
instance of	wds:Q100952417-8f487642-47c7-d880-b1e4-fc2aeed61ffe
instance of	Homo sapiens
Google Knowledge Graph ID	wds:Q100952417-7d4eaf15-4e81-e381-ca54-8eb9b9eddaad
Google Knowledge Graph ID	http://g.co/kg/g/11f37j43c6
Google Knowledge Graph ID	/g/11f37j43c6
occupation	wds:Q100952417-2c8de69e-4d05-8876-db45-b106e4879a9d
employer	wds:Q100952417-0d5edeca-43e8-f8d7-b7fc-46396a0eba7c wds:Q100952417-64440927-4621-95af-7ec8-47c9dba4a1a1 wds:Q100952417-69b88c89-437b-2d54-eb51-f0a86c0f24ab wds:Q100952417-6c47d93d-4da5-30ff-5927-a970f4819f50 wds:Q100952417-bbe01575-42fc-7ac2-55b4-8b3a0ea18556 wds:Q100952417-c4acfaf6-4b14-de5f-3f68-c372b33369f1 wds:Q100952417-fb6f0d37-4607-2510-aa73-f12f01fb88e7
place of birth	wds:Q100952417-556301c8-4592-b8ed-5d16-1a4b4df6b3fd
sex or gender	wds:Q100952417-5552ef20-4deb-7f65-0ffd-5fbebf601a6c
educated at	wds:Q100952417-1f2cc5f5-46b7-c2c5-c308-6b962f8cb59d wds:Q100952417-97bf9fed-498e-5f18-dca4-f9460cae96e8
family name	wds:Q100952417-b9fa96e7-4d69-56b2-8348-cb01a4649a7c
occupation	researcher
employer	University of Washington Harvard University University of Rochester University of Nice Sophia Antipolis Arizona State University University of Oregon University of Nevada, Reno School of Medicine
place of birth	Baltimore
sex or gender	male
educated at	Dartmouth College University of Rochester
family name	Hecht
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q100952417
is author of	Chromosomal localization of the human genes for lipocortin I and lipocortin II A rearranged transforming gene, tre, is made up of human sequences derived from chromosome regions 5q, 17q and 18q Nonrandom chromosome breakpoints in 6q deletions Hereditary intestinal neurofibromatosis. I. A distinctive genetic disease Hereditary intestinal neurofibromatosis. II. Translocation between chromosomes 12 and 14 Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis Translocation (1;7)(p11;p11): a new myeloproliferative hematologic entity Translocation t(3;8)(p14.2;q24.1) in renal cell carcinoma affects expression of the common fragile site at 3p14(FRA3B) in lymphocytes Common region on chromosome 14 in T-cell leukemia and lymphoma Cytogenetics of malignant gliomas: I. The autosomes with reference to rearrangements Mutations of the Kirsten-ras proto-oncogene in human preleukaemia Fragile sites at 4q23 and 7q11.23 unique to bone marrow cells Seizure disorders in the fragile X chromosome syndrome Cancer in ataxia-telangiectasia patients The journal "impact factor": a misnamed, misleading, misused measure Supernumerary ring chromosomes containing chromosome 17 sequences. A specific feature of dermatofibrosarcoma protuberans? Ring 22 chromosomes in dermatofibrosarcoma protuberans are low-level amplifiers of chromosome 17 and 22 sequences Chromosome clues to acute leukemia in Down's syndrome Telomeric fusion in pre-T-cell acute lymphoblastic leukemia The Philadelphia chromosome: a model of cancer and molecular cytogenetics Loss of common 3p14 fragile site expression in renal cell carcinoma with deletion breakpoint at 3p14 The fragile X chromosome: Current methods Histiocytic lymphoma cell lines: immunologic and cytogenetic studies Robertsonian chromosome recombinants are rare in cancer Prenatal detection of de novo paracentric inversion 46, XX inv (14) (q22q32.1) in a normal child: report and review of the literature Fragile sites, cancer chromosome breakpoints, and oncogenes all cluster in light G bands. New common fragile sites Clinical and biologic characterization of T-cell neoplasias with rearrangements of chromosome 7 band q34 A guide to fragile sites on human chromosomes Parental chromosome 11 alleles in Wilms tumor Fragile sites limited to lymphocytes: molecular recombination and malignancy Rare and polymorphic fragile sites and cancer Fragile sites and chromosome breakpoints in constitutional rearrangements II. Spontaneous abortions, stillbirths and newborns Fragile sites and chromosome breakpoints in constitutional rearrangements I. Amniocentesis Chromosome 5q35 breakpoint in malignant histiocytosis Fibrous histiocytoma cell line: chromosome studies of mouse and man Forebrain cleavage gene causing holoprosencephaly: deletion mapping to chromosome band 2p21. Direct prenatal chromosome diagnosis of a malignancy Chromosomes in gliomatosis cerebri. Mapping FRA11A, a folate-sensitive fragile site in human chromosome band 11q13.3. Lymphocyte subpopulation profiles and mitogen kinetics in immunological deficiency testing. Cape Malay hypospadias/mental retardation syndrome Trisomy 4 in hematologic disorders Long-term growth of malignant thymocytes in vitro. Establishment and characterization of a common acute lymphoblastic leukemia cell line with a deletion of chromosome 3 band q26. Philadelphia chromosome-positive acute lymphoblastic leukemia cell lines without classical breakpoint cluster region rearrangement Detection of the fragile X chromosome and other fragile sites. The Philadelphia (Ph) chromosome in leukemia. II. Variant Ph translocations in acute lymphoblastic leukemia Chromosome instability before cancer therapy Human somatic cell metaphase chromosome measurements

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