A patient with a mild holoprosencephaly spectrum phenotype and heterotaxy and a 1.3 Mb deletion encompassing GLI2

The molecular genetics of holoprosencephaly

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Interstitial deletion of chromosome 2q associated with ovarian dysgenesis

(2010) Everett Davis et al.   CLINICAL GENETICS

Left–right patterning in the mouse requires Epb4.1l5-dependent morphogenesis of the node and midline

(2010) Jeffrey D. Lee et al.   DEVELOPMENTAL BIOLOGY

Clinical characterization of individuals with deletions of genes in holoprosencephaly pathways by aCGH refines the phenotypic spectrum of HPE

(2010) Jill A. Rosenfeld et al.   HUMAN GENETICS

Novel Heterozygous NonsenseGLI2Mutations in Patients with Hypopituitarism and Ectopic Posterior Pituitary Lobe without Holoprosencephaly

(2010) Marcela M. França et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: An updated map of candidate loci

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Holoprosencephaly–Polydactyly syndrome: In search of an etiology

(2007) Dwight R. Cordero et al.   European Journal of Medical Genetics