Zobrazeno 1 - 8
of 8
pro vyhledávání: '"D. F. Reis"'
Publikováno v:
Brazilian Journal of Biology, Iss 0 (2018)
Abstract Macroinvertebrate shredders consume preferably leaves conditioned by fungi and bacteria which offer greater palatability to them. Plant species in Cerrado present high concentration of chemical elements such as lignin and cellulose, phenols
Externí odkaz:
https://doaj.org/article/848d8b16e09345e697cb8adb5a984232
Publikováno v:
American Journal of Medical Genetics. 44:716-719
We report on a boy with severe radial hypoplasia, absent thumbs and patellae, short stature, persistent diarrhea, slender nose and normal intelligence as another example of the RAPADILINO syndrome.
Publikováno v:
Annales de genetique. 34(2)
A de novo t(4;22)(q1200;p13) is reported in a girl with a florid 4p trisomy phenotype. The abnormal chromosome was identified by high resolution, C-bands and confirmed by 5-BrdU as de novo dicentric translocated chromosome.
Autor:
J C, de Almeida, J C, Llerena, R, Rita Martins, M, Jung, D F, Reis, A G, Cunha, D, Molina Gomes
Publikováno v:
Annales de genetique. 28(1)
A pair of monozygotic twins with Turner's syndrome was studied using combined cytogenetic techniques and a mos 45,X/46,X,r(Y) was demonstrated in both. One of the twins presented clitoral hypertrophy. Surgery was performed and uterus, bilateral Fallo
Publikováno v:
Annales de genetique. 32(3)
The authors present the clinical and cytogenetic studies of a white malformed baby with dup (3p) secondary to the malsegregation of a maternal balanced (X;3) (p22.3;p21) translocation. Besides the typical clinical features he also presented polydacty
Publikováno v:
Annales de genetique. 29(2)
mos 45,X/46,X,Y with no bright fluorescence was studied in 4 patients presenting variable phenotypes, from Turner's syndrome, with or without virilization, to ambiguous external genitalia, with combined cytogenetic techniques. G-11 staining demonstra
Publikováno v:
Annales de genetique. 32(3)
Another example of del (17)(p11.2) in a 3-year-old boy with psychomotor retardation, broad face, midface hypoplasia, prognathism, and behavioural anomalies was diagnosed clinically and confirmed by prometaphase analysis. It seems that this new microd
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