Zobrazeno 1 - 7
of 7
pro vyhledávání: '"T. D. Howard"'
Autor:
V, Shashi, P, Xie, K, Schoch, D B, Goldstein, T D, Howard, M N, Berry, C E, Schwartz, K, Cronin, S, Sliwa, A, Allen, A C, Need
Publikováno v:
Clinical genetics. 88(4)
A novel X-linked intellectual disability (XLID) syndrome with moderate intellectual disability and distinguishing craniofacial dysmorphisms had been previously mapped to the Xq26-q27 interval. On whole exome sequencing in the large family originally
Autor:
D. W. Bowden, M. Sale, T. D. Howard, A. Qadri, B. J. Spray, C. B. Rothschild, G. Akots, S. S. Rich, B. I. Freedman
Publikováno v:
Diabetes. 46:882-886
Autor:
R, Das Chakraborty, D, Chakraborty, A J, Bernal, K, Schoch, T D, Howard, E H, Ip, S R, Hooper, M S, Keshavan, R L, Jirtle, V, Shashi
Publikováno v:
Translational Psychiatry
Chromosome 22q11.2 deletion syndrome (22q11DS) is the most common microdeletion syndrome in humans. It is typified by highly variable symptoms, which might be explained by epigenetic regulation of genes in the interval. Using computational algorithms
Autor:
V, Shashi, M S, Keshavan, T D, Howard, M N, Berry, M J, Basehore, E, Lewandowski, T R, Kwapil
Publikováno v:
Clinical genetics. 69(3)
Chromosome 22q11.2 deletion syndrome (22q11DS) is a common microdeletion syndrome associated with a markedly elevated risk of schizophrenia in adulthood. Cognitive impairments such as a low IQ and deficits in attention and executive function are comm
Publikováno v:
Photosynthesis research. 74(2)
This paper presents a concise review of the structural factors which control the energy of the Q(y) absorption band of bacteriochlorophyll a in purple bacterial antenna complexes. The energy of these Q(y) absorption bands is important for excitation
Autor:
M M, Sale, T, Akamizu, T D, Howard, T, Yokota, K, Nakao, T, Mori, H, Iwasaki, S S, Rich, J E, Jennings-Gee, M, Yamada, D W, Bowden
Publikováno v:
Proceedings of the Association of American Physicians. 109(5)
To examine the genetic contribution of the thyroid-stimulating hormone receptor (TSHR, or thyrotropin receptor) gene to autoimmune thyroid disease (AITD), we identified a dinucleotide repeat polymorphism near the TSHR gene that mapped to an 8.6 cM in
Publikováno v:
ChemInform. 19