نتایج جستجو برای: duane syndrome

تعداد نتایج: 622107  

Journal: :Proceedings of the National Academy of Sciences 1924

2002
Duane Swank Sven Steinmo

Earlier versions of this paper were presented at the 1999 Annual Meeting of the American Political Science Association, September 1-5, Atlanta, GA, and the 2000 Annual Meeting of the Midwest Political Science Association, April 27-30, Chicago, IL. The authors thank Steffen Ganghof, Philip Genschel, Mark Hallerberg, Alex Hicks, William Keech, Dennis Quinn, and the anonymous reviewers and editor ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2005
G L Clark W Duane

1 Duane and Patterson, Proc. Nat. Acad. Sci., Washington, Sept. 1920; Phys. Rev., Dec. 1920, p. 526. 2 Coster, Z. Phys., 5, 1921 (139); also 6, 1921 (185). 3 De Broglie and Dauvillier, Paris, C. R., 173, p. 137. Dauvillier, Ibid., 172, also 173, p. 647, also other papers in this volume. 4 Smfkal, Z. Phys., 5, 1921 (91, 121). Also 4, 1921. 5Wentzel, Ibid., 6, 1921 (2). Coster, Ibid., 5, 1921 (14...

2016
Alexander Duane

Fuchs. Translated by Alexander Duane. .Fp. 908. Illustrations 441. Published by J. B. Lippincott & Company. There is small need to recommed a now edition of this well-known and well-appreciated work. The third English, the edition under review, is an authorised translation from the eleventh German. Alterations are numerous, especially in the sections on diseases of the cornea, iritis sympatheti...

Journal: :Revista Argentina de Radiología 2017

2013
Zouheir Hafidi Rajae Daoudi

Le syndrome de Goldenhar ou dysplasie oculo-auriculo-vertébrale est un syndrome polymalformatif rare, en rapport avec une anomalie de développement des premiers arcs branchiaux ; il est le plus souvent unilatéral affectant les tissus mous et dans une moindre proportion le tissu osseux, associant de façon variable des malformations squelettiques, auditives et oculaires avec un retard mental. Son...

Journal: :Journal of medical genetics 1993
J Burn A Takao D Wilson I Cross K Momma R Wadey P Scambler J Goodship

The conotruncal anomaly face syndrome was described in a Japanese publication in 1976 and comprises dysmorphic facial appearance and outflow tract defects of the heart. The authors subsequently noted similarities to Shprintzen syndrome and DiGeorge syndrome. Chromosome analysis in five cases did not show a deletion at high resolution, but fluorescent in situ hybridisation using probe DO832 show...

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