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	1.	Type 1 Arnold-Chiari malformation and Noonan syndrome. A new diagnostic feature? [electronic resource] by Holder-Espinasse, Muriel Winter, Robin M Producer: 20040527 In: Clinical dysmorphology vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Three craniosynostotic patients with tracheal sleeve. [electronic resource] by Okajima, Kazuki Aoki, Ichiro Sagehashi, Nobuyuki Malcolm, Sue Winter, Robin M Producer: 20030425 In: Clinical dysmorphology vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	No evidence for submicroscopic 22qter deletions in patients with features suggestive for Angelman syndrome. [electronic resource] by de Vries, Bert B A Tyson, Jess Winter, Robin M Malcolm, Sue Producer: 20020828 In: American journal of medical genetics vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	The appearance of the feet in Pfeiffer syndrome caused by FGFR1 P252R mutation. [electronic resource] by Rossi, Massimiliano Jones, Rachel L Norbury, Gail Bloch-Zupan, Agnès Winter, Robin M Producer: 20040527 In: Clinical dysmorphology vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Complex chromosomal rearrangement and associated counseling issues in a family with Pelizaeus-Merzbacher disease. [electronic resource] by Woodward, Karen Cundall, Maria Palmer, Rodger Surtees, Robert Winter, Robin M Malcolm, Sue Producer: 20031023 In: American journal of medical genetics. Part A vol. 118A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Septo-optic dysplasia, subglottic stenosis and skeletal abnormalities: a case report. [electronic resource] by Wakeling, Emma L Dattani, Mehul T Bloch-Zupan, A Winter, Robin M Holder, Susan E Producer: 20031224 In: Clinical dysmorphology vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Pseudodominant inheritance of Langer mesomelic dysplasia caused by a SHOX homeobox missense mutation. [electronic resource] by Shears, Deborah J Guillen-Navarro, Encarna Sempere-Miralles, Manuel Domingo-Jimenez, Rosario Scambler, Peter J Winter, Robin M Producer: 20020920 In: American journal of medical genetics vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Okihiro syndrome is caused by SALL4 mutations. [electronic resource] by Kohlhase, Jürgen Heinrich, Marielle Schubert, Lucia Liebers, Manuela Kispert, Andreas Laccone, Franco Turnpenny, Peter Winter, Robin M Reardon, William Producer: 20030416 In: Human molecular genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases. [electronic resource] by Siitonen, H Annika Kopra, Outi Kääriäinen, Helena Haravuori, Henna Winter, Robin M Säämänen, Anna-Marja Peltonen, Leena Kestilä, Marjo Producer: 20040622 In: Human molecular genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Different mutations in the NF1 gene are associated with Neurofibromatosis-Noonan syndrome (NFNS). [electronic resource] by Baralle, Diana Mattocks, Chris Kalidas, Kamini Elmslie, Frances Whittaker, Joanne Lees, Melissa Ragge, Nicola Patton, Michael A Winter, Robin M ffrench-Constant, Charles Producer: 20031224 In: American journal of medical genetics. Part A vol. 119A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	A locus for bilateral perisylvian polymicrogyria maps to Xq28. [electronic resource] by Villard, Laurent Nguyen, Karine Cardoso, Carlos Martin, Christa Lese Weiss, Ann M Sifry-Platt, Mara Grix, Arthur W Graham, John M Winter, Robin M Leventer, Richard J Dobyns, William B Producer: 20020418 In: American journal of human genetics vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	3D analysis of facial morphology. [electronic resource] by Hammond, Peter Hutton, Tim J Allanson, Judith E Campbell, Linda E Hennekam, Raoul C M Holden, Sean Patton, Michael A Shaw, Adam Temple, I Karen Trotter, Matthew Murphy, Kieran C Winter, Robin M Producer: 20041019 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)
	13.	Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16. [electronic resource] by Chang, Bernard S Piao, Xianhua Bodell, Adria Basel-Vanagaite, Lina Straussberg, Rachel Dobyns, William B Qasrawi, Bassam Winter, Robin M Innes, A Micheil Voit, Thomas Grant, P Ellen Barkovich, A James Walsh, Christopher A Producer: 20030604 In: Annals of neurology vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	G protein-coupled receptor-dependent development of human frontal cortex. [electronic resource] by Piao, Xianhua Hill, R Sean Bodell, Adria Chang, Bernard S Basel-Vanagaite, Lina Straussberg, Rachel Dobyns, William B Qasrawi, Bassam Winter, Robin M Innes, A Micheil Voit, Thomas Ross, M Elizabeth Michaud, Jacques L Déscarie, Jean-Claude Barkovich, A James Walsh, Christopher A Producer: 20040422 In: Science (New York, N.Y.) vol. 303 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein. [electronic resource] by McGregor, Lesley Makela, Ville Darling, Susan M Vrontou, Sofia Chalepakis, Georges Roberts, Catherine Smart, Nicola Rutland, Paul Prescott, Natalie Hopkins, Jason Bentley, Elizabeth Shaw, Alison Roberts, Emma Mueller, Robert Jadeja, Shalini Philip, Nicole Nelson, John Francannet, Christine Perez-Aytes, Antonio Megarbane, Andre Kerr, Bronwyn Wainwright, Brandon Woolf, Adrian S Winter, Robin M Scambler, Peter J Producer: 20030703 In: Nature genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)