Zobrazeno 1 - 10
of 145
pro vyhledávání: '"Edwards, Y H"'
Autor:
Blake, D. J., Schofield, J. N., Zuellig, R. A., Górecki, D. C., Phelps, S. R., Barnard, E. A., Edwards, Y. H., Davies, K. E.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1995 Apr . 92(9), 3697-3701.
Externí odkaz:
https://www.jstor.org/stable/2367413
Autor:
March, R. E., Putt, W., Hollyoake, M., Ives, J. H., Lovegrove, J. U., Hopkinson, D. A., Edwards, Y. H., Whitehouse, D. B.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1993 Nov . 90(22), 10730-10733.
Externí odkaz:
https://www.jstor.org/stable/2363301
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1977 Feb 01. 74(2), 698-701.
Externí odkaz:
https://www.jstor.org/stable/66260
Autor:
Love, D. R., Morris, G. E., Ellis, J. M., Fairbrother, U., Marsden, R. F., Bloomfield, J. F., Edwards, Y. H., Slater, C. P., Parry, D. J., Davies, K. E.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1991 Apr . 88(8), 3243-3247.
Externí odkaz:
https://www.jstor.org/stable/2356713
Autor:
Whitehouse, D. B., Putt, W., Lovegrove, J. U., Morrison, K., Hollyoake, M., Fox, M. F., Hopkinson, D. A., Edwards, Y. H.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1992 Jan 01. 89(1), 411-415.
Externí odkaz:
https://www.jstor.org/stable/2358547
Autor:
Sood, R., Bader, P. I., Speer, M. C., Edwards, Y. H., Eddings, E. M., Blair, R. T., Hu, P., Faruque, M. U., Robbins, C. M., Zhang, H., Leuders, J., Morrison, K., Thompson, D., Schwartzberg, P. L., Meltzer, P. S., Trent, J. M.
Here we report on a male patient with sacral dysgenesis (SD) and constitutional pericentric inversion of chromosome 6 (p11.2;q23.3). SD is a heterogeneous group of congenital anomalies with complex genetic etiology. Previously, a patient with sacral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2659::4655032738516ca61fcf38069e61774c
https://zenodo.org/record/1235331
https://zenodo.org/record/1235331
Publikováno v:
Scopus-Elsevier
Sacral agenesis is a heterogeneous group of congenital anomalies in which most cases are sporadic but rare familial forms also occur. Although one gene has been mapped to chromosome 7q36 in families with hemisacrum, associated with anorectal atresia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e8a30f6792dad78a72cd1347faa5ebbc
https://europepmc.org/articles/PMC1734318/
https://europepmc.org/articles/PMC1734318/
Publikováno v:
Annals of Human Genetics; Mar2004, Vol. 68 Issue 2, p85-92, 8p
Publikováno v:
Animal Genetics; Feb2001, Vol. 32 Issue 1, p32-36, 5p