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Clinical Dysmorphology|June 7, 2007
Adams-Oliver syndrome: further evidence of an autosomal recessive variantSamia A Temtamy, Mona S Aglan, Adel M Ashour, et al.
Clinical Dysmorphology|June 7, 2007
Parkes Weber syndrome occurring in a family with capillary malformationsNicola Brunetti-Pierri, Glen F Seidel, Moise L Levy, et al.
Clinical Dysmorphology|June 7, 2007
A novel mutation in TRIM37 is associated with mulibrey nanism in a Turkish boyTümay Doğancı, Berrin E Yüksel Konuk, Nursel Alpan, et al.
Clinical Dysmorphology|June 7, 2007
Antenatal diagnosis of deletion chromosome 11(q23-qter) (Jacobsen syndrome)Patricia Foley, Fionnuala McAuliffe, Marice Mullarkey, et al.
Clinical Dysmorphology|June 7, 2007
Velocardiofacial syndrome with a rare t(2;22)Jair Huber, Claudia A Rainho, Marcus V Gomes, et al.
Clinical Dysmorphology|July 31, 2010
A MID1 mutation associated with reduced penetrance of X-linked Opitz G/BBB syndromeMariken Ruiter, Erik-Jan Kamsteeg, Germana Meroni, et al.
Clinical Dysmorphology|May 11, 2010
Familial 3q29 microdeletion syndrome providing further evidence of involvement of the 3q29 region in bipolar disorderJill Clayton-Smith, Carol Giblin, Rupert A Smith, et al.
Clinical Dysmorphology|September 6, 2007
Alagille syndrome with deletion 20p12.2-p12.3 and hypoplastic left heartMarie Leema P Robert, Tony Lopez, John Crolla, et al.
Clinical Dysmorphology|September 6, 2007
Midline defects in deletion 18p syndrome: clinical and molecular characterization of three patientsMarie-France Portnoï, Nicolas Gruchy, Sandrine Marlin, et al.
Clinical Dysmorphology|September 6, 2007
Mutations and new polymorphic changes in the TCOF1 gene of patients with oculo-auriculo-vertebral spectrum and Treacher-Collins syndromePen-Hua Su, Ju-Shan Yu, Jia-Yuh Chen, et al.
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