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Serveur d'exploration sur le lymphœdème - Analysis (France)

Index « ISSN » - entrée « 1097-0223 »
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1097-0142 < 1097-0223 < 1097-0347  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 14.
Ident.Authors (with country if any)Title
000185 (2013) A. Gaudineau [France] ; B. Doray [France] ; E. Schaefer [France] ; N. Sananès [France] ; G. Fritz [France] ; M. Kohler [France] ; Y. Alembik [France] ; B. Viville [France] ; R. Favre [France] ; B. Langer [France]Postnatal phenotype according to prenatal ultrasound features of Noonan syndrome: a retrospective study of 28 cases
000186 (2013) Juliette Beaujot [France] ; Sylvie Joriot [France] ; Anne Dieux [France] ; Pascal Vaast [France] ; Hélène Franquet-Ansart [France] ; Anne-Sylvie Valat [France] ; Philippe Deruelle [France] ; Muriel Holder-Espinasse [France] ; Louise Devisme [France]Phenotypic variability of prenatally presenting Gaucher's disease
000243 (2012) J. M. Pellegrinelli [Suisse, France] ; A. Kohler [France] ; M. Kohler [France] ; A. S. Weingertner [France] ; R. Favre [France]Prenatal management and thoracoamniotic shunting in primary fetal pleural effusions: a single centre experience
000297 (2011) J. Benard [France] ; J. Saada [France] ; J. Amiel [France] ; S. Vignes [France] ; A. Benachi [France] ; O. Picone [France]Prenatal diagnosis of Milroy disease
000395 (2009) P. Callier [France] ; L. Faivre [France] ; S. Pigeonnat [France] ; B. Quilichini [France] ; N. Marle [France] ; C. Thauvin-Robinet [France] ; A. L. Mosca [France] ; A. Masurel-Paulet [France] ; T. Rousseau [France] ; P. Sagot [France] ; N. Laurent [France] ; F. Mugneret [France]Contribution of array CGH in prognosis and genetic counselling of prenatally diagnosed supernumerary ring chromosome 20
000501 (2006) Jean-Marc Levaillant [France] ; Marion Gérard-Blanluet [France] ; Muriel Holder-Espinasse [France] ; Anne-Sylvie Valat-Rigot [France] ; Louise Devisme [France] ; Hélène Cavé [France] ; Sylvie Manouvrier-Hanu [France]Prenatal phenotypic overlap of Costello syndrome and severe Noonan syndrome by tri‐dimensional ultrasonography
000502 (2006) Logos Curtis [Suisse] ; Eric Antonelli [Suisse] ; Yvan Vial [Suisse] ; Peter Rimensberger [Suisse] ; Martine Le Merrer [France] ; Christine Hinard [Suisse] ; Armand Bottani [Suisse] ; Siv Fokstuen [Suisse]Prenatal diagnostic indicators of paternal uniparental disomy 14
000505 (2006) Olivier Picone [France] ; Raphaël Hirt [France] ; Sophie Brisset [France] ; René Frydman [France] ; Marie-Victoire Senat [France] ; Gérard Tachdjian [France]Double aneuploid mosaicism 45,X/46,XX/47,XX,+18 in a fetus with cerebral malformations
000595 (2004) Jean-Luc Brun [France] ; Flore Gangbo [France] ; Zon Qi Wen [France] ; Katia Galant [France] ; Laurence Taine [France] ; Brigitte Maugey-Laulom [France] ; Denis Roux [France] ; Raphaelle Mangione [France] ; Jacques Horovitz [France] ; Robert Saura [France]Prenatal diagnosis and management of sex chromosome aneuploidy: a report on 98 cases
000598 (2004) L. Sentilhes [France] ; E. Verspyck [France] ; D. Eurin [France] ; V. Ickowicz [France] ; S. Patrier [France] ; J. Lechevallier [France] ; L. Marpeau [France]Favourable outcome of a tight constriction band secondary to amniotic band syndrome
000623 (2003) S. Eva Pannier [France] ; G. Viot [France] ; M. C. Aubry [France] ; G. Grange [France] ; J. Tantau [France] ; C. Fallet-Bianco [France] ; F. Muller [France] ; D. Cabrol [France]Congenital erythropoietic porphyria (Günther's disease): two cases with very early prenatal manifestation and cystic hygroma
000658 (2002) B. Gilbert [France] ; C. Yardin [France] ; S. Briault [France] ; V. Belin [France] ; A. Lienhardt [France] ; Y. Aubard [France] ; J. Battin [France] ; M. Servaud [France] ; H. J. Philippe [France] ; D. Lacombe [France]Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counselling
000716 (2001) P. Schw Rzler [Royaume-Uni, Autriche] ; T. Homfray [Royaume-Uni] ; S. Campbell [Royaume-Uni] ; Y. Ville [Royaume-Uni, France]Prenatal findings on ultrasound and X‐ray in a case of overgrowth syndrome associated with increased nuchal translucency
000800 (1999) Françoise Muller [France] ; Sandrine Ngo [France] ; Maryneige Rebiffé [France] ; Jean-François Oury [France] ; Serge Uzan [France] ; Daniel Satgé [France]Maternal serum s100b protein is ineffective for Down syndrome screening

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