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Scholar Results 1 - 7 of 7 citing Lloyd: Anterior segment dysgenesis in mosaic Turner syndrome. (0.08 sec) 

Phenotypic effects of mosaicism for a 47, XXX cell line in Turner syndrome

- bmj.com [PDF] 
VP Sybert - British Medical Journal, 2002 - jmg.bmj.com
T he brachydactylies are a group of inherited disorders characterised by shortened or malformed
digits that are thought to be the result of abnormal growth of the phalanges and/or metacarpals.
First classified by Bell into types ...
Cited by 11 - Related articles - BL Direct - All 7 versions

Ophthalmic features of Turner's syndrome


AKO Denniston, L Butler - Eye, 2004 - nature.com
Turner's syndrome is one of the most common of all chromosomal abnormalities and is associated with
significant ophthalmic morbidity. Turner's 1938 account included two patients with strabismus, and
hitherto the condition has ...
Cited by 6 - Related articles - All 3 versions

Turner's syndrome


A Denniston - The Lancet, 2001 - Elsevier
By contrast, Lloyd and colleagues 4 did a careful ophthalmic and chromosomal examination of four
girls with mosaic Turner's syndrome. They noted anterior-segment abnormalities, including glaucoma
and abnormal irides (Rieger ...
Cited by 2 - Related articles - BL Direct - All 3 versions

Ophthalmological and otological problems in Turner syndrome

- turner-forening.dk [PDF] 
P Saenger, H Nussbaum, B Lippe - International Congress Series, 2006 - Elsevier
Hearing problems and ear malfunctions are also common in TS and correlate with the karyotype. As a
result of the frequent otitis media, conductive hearing loss is common in girls with TS.
Sensorineural hearing loss is also ...
Cited by 1 - Related articles - All 3 versions

Uveitis in Turner's syndrome


M Accorinti, M La Cava, S Speranza, P Pivetti- … - Graefe's Archive for Clinical …, 2002 - Springer
Abstract Background: Turner's syndrome is a chromosomal abnor- mality where phenotypic females have
either a missing X chromosome or a structural aberration of the X chromosome. Several ocular
diseases have been associated with ...
Cited by 1 - Related articles - BL Direct - All 3 versions

[PDF] Co ex is tence of Go nadal Dysgenesis and Mullerian Agenesis with Two Mo saic …


TC Ting, SP Chang - homepage.vghtpe.gov.tw
Go nadal dysgenesis and Mullerian agenesis both are com mon causes of pri mary amenorrhea. Co - ex
is tence of go nadal dysgenesis and Mullerian agenesis has been pre vi ously de scribed as a rare
event. Go nadal dysgenesis in ...
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[PDF] ОФТАЛМОЛОШКЕ ПРОМЕНЕ КОД ТУРНЕРОВОГ СИНДРОМА


EYESINTS SYNDROME - Clinic - med.pr.ac.rs
1Клиника за Очне болести, Медицински факултет
Приштина, Косовска Митровица 2Интерна клиника,
Медицински ...
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