نتایج جستجو برای: yunis

تعداد نتایج: 53  

Journal: :Journal of Human Genetics 2013

Journal: :Journal of Medical Genetics 1989

Journal: :Journal of medical genetics 1989
R C Hennekam C Vermeulen-Meiners

A boy with intrauterine growth retardation, microcephaly, dysostosis of the skull, hypoplastic facial bones, labiogingival retraction, agenesis of the clavicles, distal aphalangia, and severely hypoplastic thumbs and halluces is described. The features are consistent with the Yunis-Varon syndrome. Review of published reports shows this to be a generalised disorder with variable manifestations i...

Journal: :Akra kültür sanat ve edebiyat dergisi 2021

Makalede büyük Hüseyin Cavid'in 'Topal Timur' tiyatro oyunu sanatsal ve tarihsel açıdan değerlendiriliyor. Bu eserinin Özbekistan`ın sanat ortamına katkısı, aynı zamanda bağımsızlık döneminde Azerbaycan Özbek edebiyatında Amir Timur imgesinin oluşumu gibi konular ele alınıyor. düşünürü Abdürrauf Fıtrat, Abdullah Aripov, Siracedin Seyyid çağdaş romanlarının ünlü yazarı Yunis Oguz sanatında özell...

Journal: :Annals of the rheumatic diseases 1963
M WILKINSON B S JONES

Although first described in 1951 (Polley and Bickel, 1951), needle biopsy of synovial membrane has not come into such common usage as that of liver, pleura, or even kidney. Judging from the few American reports dealing with its diagnostic value (Mikkelsen, Duff, Castor, Zevely, and French, 1958; Polley, Bickell and Dockerty, 1954; Rodnan, Yunis, and Totten, 1960; Schwartz and Cooper, 1961), the...

Journal: :Journal of medical genetics 1984
P Ward S Packman W Loughman M Sparkes R Sparkes A McMahon T Gregory A Ablin

Retinoblastoma occurs with increased frequency in children born with a deletion of the long arm of chromosome 13. Recent reviews have noted that the region 13q14 is consistently deleted in documented cases. Prometaphase and late prophase banding allowed Yunis and Ramsay to determine that a deletion in one patient included the sub-bands q14 . 12, q14 . 13, and q14 . 2, and a portion of q14 . 11 ...

Journal: :Journal of medical genetics 1968
E Krmpotic K Ramanathan A Grossman

Balanced D/D translocation carriers appear to be normal in most instances (Court-Brown et al., 1966; Giannelli and Howlett, 1966). In some cases, however, a variety ofcongenital malformations has been reported, such as Klinefelter's syndrome (Lejeune, Turpin, and Decourt, 1960), little secondary sex development (Walker and Harris, 1962), malformation of the spine (de Grouchy et al., 1963), arre...

2006
P. H. FITZGERALD L. A. BREHAUT

True hermaphrodites possess both ovarian and testicular tissues which may be present in separate gonads or combined in an ovotestis. External and internal genitalia are ambiguous and variable, though a prominent penial structure is usual. Chromosome examination of true hermaphroditism has revealed an XX sex chromosome complement in the majority of cases, but the XY complement and different mosa...

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