Karyotype < Karyotyping < Kasabach-Merritt Syndrome

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List of bibliographic references indexed by Karyotyping

Number of relevant bibliographic references: 37.
[20-40] [0 - 20][0 - 37]

Ident.	Authors (with country if any)	Title
00AD75 (1999)	A. Tsezou ; Ch Hadjiathanasiou ; D. Gourgiotis ; A. Galla ; Em Kavazarakis ; A. Pasparaki ; M. Kapsetaki ; C. Sismani [Chypre (pays)] ; Ch Theodoridis ; Pc Patsalis [Chypre (pays)] ; N. Moschonas ; S. Kitsiou	Molecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy
00AE54 (1999)	David Mowat [Australie] ; Anna Jauch [Allemagne] ; Lisa Robson [Australie] ; Arabella Smith [Australie]	Duplication within chromosome 5q characterized by fluorescence in situ hybridization
00B702 (1997)	J L Ruibal Francisco [Espagne] ; P. Sánchez Bur N ; E. Pi Ero Martínez ; G. Bueno Lozano ; F. Reverte Blanc	[Turner's syndrome. Relationship between the karyotypes and malformations and associated diseases in 23 patients].
00C881 (1994)	M. Genuardi [Italie] ; F. Calvieri ; C. Tozzi ; R. Coslovi ; G. Neri	A new case of interstitial deletion of chromosome 3q, del(3q)(q13.12q21.3), with agenesis of the corpus callosum.
00CC66 (1993)	R. Greenlee ; H. Hoyme ; M. Witte ; P. Crowe ; C. Witte	Developmental disorders of the lymphatic system.
00D457 (1991)	S. Douvier ; J P Feldman ; A. Nivelon-Chevalier ; M. Degrolard ; M H Harran ; J. Jahier	[Retrocervical cystic hygroma: diagnosis, prognosis and management. A series of 13 cases].
00D499 (1991)	L. Zelante [Italie] ; F. Torricelli ; S. Calvano ; R. Mingarelli ; B. Dallapiccola	Ring chromosome 14 syndrome. Report of two cases, including extended evaluation of a previously reported patient and review.
00D753 (1991)	Lars Gunnar Kindblom [Suède] ; Göran Stenman [Suède] ; Lennart Angervall [Suède]	Morphological and cytogenetic studies of angiosarcoma in Stewart-Treves syndrome
00D963 (1990)	J C Chang [République populaire de Chine] ; T T Sun	Ultrasonographic diagnosis of fetal cystic hygroma.
00DF67 (1989)	Natalie Blagowidow [États-Unis] ; David C. Page ; Dale Huff [États-Unis] ; Michael T. Mennuti [États-Unis]	Ullrich‐Turner syndrome in an XY female fetus with deletion of the sex‐determining portion of the Y chromosome
00E192 (1988)	P. Sarda [France] ; J. Jalaguier ; F. Montoya ; H. Bonnet	[Hereditary congenital lymphedema with pseudosexual ambiguity].
00E920 (1986)	H J Voigt ; U. Claussen ; R. Ulmer	[Fetal neck edema--early sonographic indications of a chromosome abnormality].
011296 (1966)	R A Ersek ; C A Danese ; J M Howard	Hereditary congenital lymphedema (Milroy's disease).
012666 (????)	C H Gonzalez ; H B Corradini ; P H Saladanha	[Identification of Turner's syndrome in the newborn infant].
012790 (????)	D. Simm [Allemagne] ; K. Degenhardt ; C. Gerdemann ; T M K. Völkl ; A. Rauch ; H G Dörr	[Chronological age of patients with Turner syndrome at diagnosis].
012A06 (????)	C. Severien ; S. Felix ; K. Bartholomé	Ring chromosome 22: a case report.
012C06 (????)	W. Minkin ; S B Frank ; S R Wolman ; H J Cohen	Lymphedema in Noonan's syndrome.

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