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	881.	Chromosome 6p25 deletion syndrome: report of a case with optic disc coloboma and review of published ophthalmic findings. [electronic resource] by Beby, Francis Des Portes, Vincent Till, Marianne Mottolese, Carmine Denis, Philippe Producer: 20130326 In: Ophthalmic genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	882.	Neuropsychological and behavioural phenotype of Dandy-Walker variant presenting in chromosome 22 trisomy: a case study. [electronic resource] by Searson, Ruth Hare, Dougal Julian Sridharan, Sridhar Producer: 20140123 In: Journal of intellectual disabilities : JOID vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	883.	Revised classification of posterior fossa cysts and cystlike malformations based on the results of multiplanar MR imaging. [electronic resource] by Barkovich, A J Kjos, B O Norman, D Edwards, M S Producer: 19891218 In: AJR. American journal of roentgenology vol. 153 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	884.	Homozygous mutations in the plasminogen gene of two unrelated girls with ligneous conjunctivitis. [electronic resource] by Schuster, V Mingers, A M Seidenspinner, S Nüssgens, Z Pukrop, T Kreth, H W Producer: 19970825 In: Blood vol. 90 Availability: No items available. Save to lists Add to cart (remove)
	885.	Increased nuchal translucency thickness: a potential indicator for Ritscher-Schinzel syndrome. [electronic resource] by Rusnak, Alison J Hadfield, Marie I Chudley, Albert E Marles, Sandra L Reid, Gregory J Chodirker, Bernard N Producer: 20090413 In: Fetal diagnosis and therapy vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	886.	Familial occurrence of isolated Dandy-Walker variant in two consecutive male fetuses. [electronic resource] by Lin, Y H Chen, C P Chen, T C Liang, S J Hsu, C S Producer: 20070508 In: Genetic counseling (Geneva, Switzerland) vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	887.	Discrepancy in fetal sex assignment between cell free fetal DNA and ultrasound. [electronic resource] by Iruretagoyena, J I Grady, M Shah, D Producer: 20151130 In: Journal of perinatology : official journal of the California Perinatal Association vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	888.	Prenatal diagnosis of trisomy 9 mosaic presenting as a case of Dandy-Walker malformation. [electronic resource] by Bureau, Y A Fraser, W Fouquet, B Producer: 19930504 In: Prenatal diagnosis vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	889.	Phenotypical variation in cousins with the identical partial trisomy 9 (pter-q22.2) and 7 (q35-qter) at 16 and 23 weeks gestation. [electronic resource] by Metzke-Heidemann, S Kuhling-von Kaisenberg, H Caliebe, A Janssen, D Jonat, W Grote, W von Kaisenberg, C S Producer: 20040503 In: American journal of medical genetics. Part A vol. 126A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	890.	Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions. [electronic resource] by Ferraris, Alessandro Bernardini, Laura Sabolic Avramovska, Vesna Zanni, Ginevra Loddo, Sara Sukarova-Angelovska, Elena Parisi, Valentina Capalbo, Anna Tumini, Stefano Travaglini, Lorena Mancini, Francesca Duma, Filip Barresi, Sabina Novelli, Antonio Mercuri, Eugenio Tarani, Luigi Bertini, Enrico Dallapiccola, Bruno Valente, Enza Maria Producer: 20140102 In: Orphanet journal of rare diseases vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	891.	Prenatal diagnosis of posterior fossa anomalies: Additional value of chromosomal microarray analysis in fetuses with cerebellar hypoplasia. [electronic resource] by Zou, Zhiyong Huang, Linhuan Lin, Shaobin He, Zhiming Zhu, Hui Zhang, Yi Fang, Qun Luo, Yanmin Producer: 20181108 In: Prenatal diagnosis vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	892.	Posterior fossa abnormalities in children with infantile spasms. [electronic resource] by Schiffmann, R Mannheim, G B Stafstrom, C E Hamburger, S D Holmes, G L Producer: 19931222 In: Journal of child neurology vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	893.	Cystic retrocerebellar malformations: unification of the Dandy-Walker complex and the Blake's pouch cyst. [electronic resource] by Strand, R D Barnes, P D Poussaint, T Y Estroff, J A Burrows, P E Producer: 19931109 In: Pediatric radiology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	894.	De novo pure 12q22q24.33 duplication: first report of a case with mental retardation, ADHD, and Dandy-Walker malformation. [electronic resource] by Cappellacci, S Martinelli, S Rinaldi, R Martinelli, E Parisi, P Mancini, B Pescosolido, R Grammatico, P Producer: 20060727 In: American journal of medical genetics. Part A vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	895.	A 12 Mb deletion of 6p24.1-->pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneys. [electronic resource] by Chen, Chih-Ping Tzen, Chin-Yuan Chern, Schu-Rern Tsai, Fuu-Jen Hsu, Chin-Yuan Lee, Chen-Chi Lee, Meng-Shan Pan, Chen-Wen Wang, Wayseen Producer: 20090428 In: European journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	896.	Multiple developmental programs are altered by loss of Zic1 and Zic4 to cause Dandy-Walker malformation cerebellar pathogenesis. [electronic resource] by Blank, Marissa C Grinberg, Inessa Aryee, Emmanuel Laliberte, Christine Chizhikov, Victor V Henkelman, R Mark Millen, Kathleen J Producer: 20110502 In: Development (Cambridge, England) vol. 138 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	897.	Holoprosencephaly with cerebellar vermis hypoplasia in 13q deletion syndrome: Critical region for cerebellar dysgenesis within 13q32.2q34. [electronic resource] by Mimaki, Masakazu Shiihara, Takashi Watanabe, Mio Hirakata, Kyoko Sakazume, Satoru Ishiguro, Akio Shimojima, Keiko Yamamoto, Toshiyuki Oka, Akira Mizuguchi, Masashi Producer: 20160310 In: Brain & development vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	898.	Smith-Lemli-Opitz syndrome - Fetal phenotypes with special reference to the syndrome-specific internal malformation pattern. [electronic resource] by Schoner, Katharina Witsch-Baumgartner, Martina Behunova, Jana Petrovic, Robert Bald, Rainer Kircher, Susanne G Ramaswamy, Annette Kluge, Britta Meyer-Wittkopf, Matthias Schmitz, Ralf Fritz, Barbara Zschocke, Johannes Laccone, Franco Rehder, Helga Producer: 20210524 In: Birth defects research vol. 112 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	899.	The "keyhole": a sign of herniation of a trapped fourth ventricle and other posterior fossa cysts. [electronic resource] by Wolfson, B J Faerber, E N Truex, R C Producer: 19870724 In: AJNR. American journal of neuroradiology vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	900.	Description of the smallest critical region for Dandy-Walker malformation in chromosome 13 in a girl with a cryptic deletion related to t(6;13)(q23;q32). [electronic resource] by Mademont-Soler, Irene Morales, Carme Armengol, Lluís Soler, Anna Sánchez, Aurora Producer: 20101215 In: American journal of medical genetics. Part A vol. 152A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1069 results.