نتایج جستجو برای: chromosome abnormalities

تعداد نتایج: 214354  

Journal: :Cancer research 1988
C A Griffin A L Hawkins R J Packer L B Rorke B S Emanuel

Recurrent, site-specific chromosome translocations and other cytogenetic abnormalities are being described in ever-increasing numbers and types of human tumors. Primary brain tumors are the most common pediatric solid tumor and differ from those of adults in both histology and clinical behavior. We examined chromosomes from 21 primary pediatric brain neoplasms grown in short-term tissue culture...

Journal: :Archives of disease in childhood 1979
D C Candy A R Hayward D T Hughes L Layward J F Soothill

Six children, with severe deficiency of some or all of the immunoglobulins and minor somatic abnormalities, had chromosomal abnormalities: (1) 45,XY,t(13q/18q), (2) 46,XY,21ps +, (3) two brothers 46,XY (inv. 7) (4) 45,X,t(11p/10p)/46X,iXq,t(11p/10p) and, (5) in addendum, 45,XX,-18;46,XX, r18. The chromosome abnormalities were detected in B- as well as T-lymphocytes (as evidenced by using both P...

Journal: :Journal of medical genetics 1970
D T Arakaki S H Waxman

2003
D. DAVIDSON N. G. Anderson

P UTRESCINE has been found to induce chromosome aberrations in cells undergoing meiosis in Oenothera [8] but not in cells undergoing mitosis in roots of Vicia faba [9]. In re-examining the action of putrescine and cadaverine in less toxic concentrations [cf. 91, we have tested the ability of these polyamines either to induce chromosome breakage or to upset the process of chromosome condensation...

Journal: :Seizure 2015
Alberto Verrotti Alessia Carelli Lorenza di Genova Pasquale Striano

PURPOSE To analyze the various types of epilepsy in subjects with chromosome 18 aberrations in order to define epilepsy and its main clinical, electroclinical and prognostic aspects in chromosome 18 anomalies. METHODS A careful overview of recent works concerning chromosome 18 aberrations and epilepsy has been carried out considering the major groups of chromosomal 18 aberrations, identified ...

Journal: :Blood 1984
J T Eppig J E Barker

Mice with the recessive hereditary disease, Hertwig's anemia (an/an), exhibit a persistent mild macrocytic anemia and reduced fertility. We examined mitotic figures from bone marrow and kidney cells of adult mice and from liver cells of fetal mice that were genetically normal or had Hertwig's anemia. Uniformly normal mitotic figures were observed in the nonanemic mice (+/+ or +/an). In contrast...

Journal: :Annals of the Academy of Medicine, Singapore 1983
J D Rowley

Nonrandom chromosome changes have been identified in a number of malignant human tumors. The leukemias are among the best studied malignant cells and they provide the largest body of relevant cytogenetic data. In chronic myeloid leukemia, a reasonably consistent translocation [t(9;22) (q34;q11)] is observed in 93 percent of all Ph1 positive patients. In the other patients, translocations are ei...

Journal: :Journal of medical genetics 1993
A Gosch R Pankau

Telvi et al' recently reported on a 27 month old girl with an unbalanced de novo translocation, t(X;21)(q28;ql 1), and diagnosed this child as having an incomplete form of Williams-Beuren syndrome (WBS). This was based on some symptoms specific to WBS, such as craniofacial dysmorphism, delayed psychomotor development, short stature, horseshoe kidneys, and a positive WBS score of + 4.09.2 We do ...

Journal: :Journal of Animal and Feed Sciences 2003

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