1097-0215 < 1097-0223 < 1097-0231

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List of bibliographic references indexed by 1097-0223

Number of relevant bibliographic references: 68.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
003A73 (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
003A86 (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
004634 (2012)	Keren Markus-Bustani [Israël] ; Yuval Yaron [Israël] ; Myriam Goldstein [Israël] ; Avi Orr-Urtreger [Israël] ; Shay Ben-Shachar [Israël]	Undetected sex chromosome aneuploidy by chromosomal microarray
004695 (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
004698 (2012)		Poster Abstracts of the ISPD 16th International Conference on Prenatal Diagnosis and Therapy
005202 (2011)	M. Bakker [Pays-Bas] ; E. Pajkrt [Pays-Bas] ; I. B. Mathijssen [Pays-Bas] ; C. M. Bilardo [Pays-Bas]	Targeted ultrasound examination and DNA testing for Noonan syndrome, in fetuses with increased nuchal translucency and normal karyotype
005249 (2011)	J. Benard [France] ; J. Saada [France] ; J. Amiel [France] ; S. Vignes [France] ; A. Benachi [France] ; O. Picone [France]	Prenatal diagnosis of Milroy disease
005C25 (2010)	Juyoung Lee [Corée du Sud] ; Dong Gyu Jang [Corée du Sud] ; Ji Young Kwon [Corée du Sud] ; Chung Sik Chun [Corée du Sud] ; Jong Chul Shin [Corée du Sud] ; In Yang Park [Corée du Sud]	Prenatal sonographic findings associated with fibroepithelial stromal polyp of the vulva
006481 (2009)	Margaret R. Hüsler [Suisse] ; R. Douglas Wilson [États-Unis] ; Steven C. Horii [États-Unis] ; Michael W. Bebbington [États-Unis] ; N. Scott Adzick [États-Unis] ; Mark P. Johnson [États-Unis]	When is fetoscopic release of amniotic bands indicated? Review of outcome of cases treated in utero and selection criteria for fetal surgery
006688 (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
006751 (2009)	Yolanda M. De Mooij [Pays-Bas] ; Nynke M. S. Van Den Akker [Pays-Bas] ; Mireille N. Bekker [Pays-Bas] ; Margot M. Bartelings [Pays-Bas] ; Lambertus J. Wisse [Pays-Bas] ; John M. G. Van Vugt [Pays-Bas] ; Adriana C. Gittenberger-De Groot [Pays-Bas]	Abnormal Shh and FOXC2 expression correlates with aberrant lymphatic development in human fetuses with increased nuchal translucency
006D23 (2008)	I. Witters [Belgique] ; E. Denayer [Belgique] ; H. Brems [Belgique] ; J. P. Fryns [Belgique] ; E. Legius [Belgique]	The cardiofaciocutaneous syndrome: prenatal findings in two patients
006D71 (2008)	Glen Brice [Royaume-Uni]	Perinatal diagnosis of a lymphoedema‐distichiasis syndrome
006E84 (2008)		Current awareness in prenatal diagnosis
006E85 (2008)		Current awareness in prenatal diagnosis
006F46 (2008)	Gwo-Chin Ma [Taïwan] ; Chin-San Liu [Taïwan] ; Shun-Ping Chang [Taïwan] ; Kun-Tu Yeh [Taïwan] ; Yu-Yuan Ke [Taïwan] ; Tze-Ho Chen [Taïwan] ; Boris Bao-Tyan Wang [Taïwan, États-Unis] ; Shou-Jen Kuo [Taïwan] ; Jin-Chung Shih [Taïwan] ; Ming Chen [Taïwan, République populaire de Chine]	A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: possible correlation with poor response to fetal therapy
007481 (2007)	Ming Chen [Taïwan] ; Chang-Yao Hsieh [Taïwan] ; Jin-Chung Shih [Taïwan] ; Chia-Hung Chou [Taïwan] ; Gwo-Chin Ma [Taïwan] ; Tze-Ho Chen [Taïwan] ; Tsung-Hsien Lee [Taïwan] ; Horng-Der Tsai [Taïwan] ; Alan D. Cameron [Royaume-Uni] ; Chih-Ping Chen [Taïwan]	Proinflammatory macrophage migratory inhibition factor and interleukin‐6 are concentrated in pleural effusion of human fetuses with prenatal chylothorax
007488 (2007)	M. Büchner [Allemagne] ; S. Dostert [Allemagne] ; A. Falkert [Allemagne] ; G. Huber [Allemagne] ; B. Seelbach-Göbel [Allemagne]	Perinatal diagnosis of a lymphedema‐distichiasis syndrome (LD)
007B70 (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
007B71 (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
007B72 (2006)	Chih-Ping Chen [Taïwan] ; Tzu-Hao Wang [Taïwan] ; Schu-Rern Chern [Taïwan] ; Chin-Yuan Tzen [Taïwan] ; Chin-Yuan Hsu [Taïwan] ; Chen-Chi Lee [Taïwan] ; Li-Feng Chen [Taïwan] ; Chung-Chun Ma [Taïwan] ; Po-Tsang Chen [Taïwan] ; Wayseen Wang [Taïwan]	Prenatal diagnosis of congenital chylothorax associated with de novopartial trisomy 12q (12q21.2→qter)

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