Turkey < Turner Syndrome < Twin Studies as Topic

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List of bibliographic references

Number of relevant bibliographic references: 79.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000210 (????)	J. Van Borsel [Belgique] ; I. Dhooge ; K. Verhoye ; K. Derde ; L. Curfs	Communication problems in Turner syndrome: a sample survey.
000221 (1999)	F. Haverkamp [Allemagne] ; J. Wölfle ; K. Zerres ; O. Butenandt ; P. Amendt ; B P Hauffa ; E. Weimann ; M. Bettendorf ; E. Keller ; R. Mühlenberg ; C J Partsch ; W G Sippell ; C. Hoppe	Growth retardation in Turner syndrome: aneuploidy, rather than specific gene loss, may explain growth failure.
000260 (1999)	A. Tsezou [Grèce] ; C. Hadjiathanasiou ; D. Gourgiotis ; A. Galla ; E. Kavazarakis ; A. Pasparaki ; M. Kapsetaki ; C. Sismani ; C. Theodoridis ; P C Patsalis ; N. Moschonas ; S. Kitsiou	Molecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy.
000461 (2000)	L. S Vendahl [Suède] ; M L Davenport	Delayed diagnoses of Turner's syndrome: proposed guidelines for change.
000639 (2001)	C A Findlay [Royaume-Uni] ; M D Donaldson ; G. Watt	Foot problems in Turner's syndrome.
000645 (2001)	O. Butenandt	[Lymphedema. In Ullrich-Turner syndrome it is congenital].
000655 (2001)	M. Sood [Inde] ; A. Trehan	Turner's syndrome in infancy.
000682 (2001)	G. Lorette [France] ; L. Vaillant ; F. Baulieu	[Lymphedema in children].
000683 (2001)	M J Karkkainen [Finlande] ; L. Jussila ; R E Ferrell ; D N Finegold ; Kari Alitalo [Finlande]	Molecular regulation of lymphangiogenesis and targets for tissue oedema.
000714 (2001)	K A Leppig [États-Unis] ; C M Disteche	Ring X and other structural X chromosome abnormalities: X inactivation and phenotype.
000754 (2001)	C. Boucher ; C. Sargent ; T. Ogata ; N. Affara	Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location
000894 (2002)	Tsutomu Ogata [Japon] ; Koji Muroya ; Goro Sasaki ; Gen Nishimura ; Hiroshi Kitoh ; Tadashi Hattori	SHOX nullizygosity and haploinsufficiency in a Japanese family: implication for the development of Turner skeletal features.
000A93 (2002)	Imad R. Makhoul [Israël] ; Polo Sujov ; Nadir Ghanem ; Moshe Bronshtein	Prenatal diagnosis of Milroy's primary congenital lymphedema.
000B36 (????)	Daniela Larizza [Italie] ; Miryam Martinetti ; Jean Michel Dugoujon ; Carmine Tinelli ; Valeria Calcaterra ; Mariaclara Cuccia ; Laura Salvaneschi ; Francesca Severi	Parental GM and HLA genotypes and reduced birth weight in patients with Turner's syndrome.
000B90 (2002)	Tsutomu Ogata [Japon]	SHOX haploinsufficiency and its modifying factors.
000D05 (????)	V S Bamrah ; K. Ajlouni ; W H Squires ; C V Hughes ; P S Rosenfeld ; F E Tristani	Aortic regurgitation and pigmentation - unusual features of Noonan syndrome.
001363 (1963)	P. Barthe	[CONGENITAL PTERYGIUM COLLI; AN UNUSUAL ASPECT OF THE DISEASE].
001567 (1965)	P. F. Benson ; M. H. Gough ; P. E. Polani	Lymphangiography and Chromosome Studies in Females with Lymphoedema and Possible Ovarian Dysgenesis
001685 (1992)	M W Austin ; A. Patterson ; R A Bates	Conjunctival lymphoedema in Turner's syndrome.
001969 (2004)	Eve J. Lowenstein [États-Unis] ; Karen H. Kim ; Sharon A. Glick	Turner's syndrome in dermatology.
001A27 (2004)	Mariam Patrícia Auada [Brésil] ; Maria Letícia Cintra ; Maria Beatriz Puzzi ; Danilo Viana ; Denise Pontes Cavalcanti	Scalp lesions in Turner syndrome: a result of lymphoedema?

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