Pages that link to "Q33597445"
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The following pages link to Focal dermal hypoplasia (Goltz syndrome). (Q33597445):
Displaying 35 items.
- Probable identity of Goltz syndrome and Van Allen-Myhre syndrome: evidence from phenotypic evolution (Q34737323) (← links)
- Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparing (Q34742831) (← links)
- Multiple requirements of the focal dermal hypoplasia gene porcupine during ocular morphogenesis (Q34780843) (← links)
- Focal dermal hypoplasia: a rare case report (Q35052314) (← links)
- A rare human syndrome provides genetic evidence that WNT signaling is required for reprogramming of fibroblasts to induced pluripotent stem cells (Q35105698) (← links)
- Deletion of mouse Porcn blocks Wnt ligand secretion and reveals an ectodermal etiology of human focal dermal hypoplasia/Goltz syndrome (Q35149624) (← links)
- Goltz syndrome: a newborn with ectrodactyly and skin lesions (Q35215283) (← links)
- A Comprehensive Overview of Skeletal Phenotypes Associated with Alterations in Wnt/β-catenin Signaling in Humans and Mice (Q35755034) (← links)
- Genetic Disorders of the Skin and Eye (Q36264290) (← links)
- Novel mutation in a child with Goltz syndrome. (Q37898015) (← links)
- Focal dermal hypoplasia: updates (Q38086832) (← links)
- Wnt Signaling in Cardiac Disease (Q38542451) (← links)
- Cognitive and psychological functioning in focal dermal hypoplasia (Q38915446) (← links)
- Recurrent digital fibroma, focal dermal hypoplasia, and limb malformations (Q39546768) (← links)
- The orthopedic characterization of Goltz syndrome (Q40004791) (← links)
- Classification of microphthalmos and coloboma (Q40864641) (← links)
- Genodermatoses in women (Q41349307) (← links)
- Lenz microphthalmic syndrome in an Indian patient (Q41939722) (← links)
- Renal coloboma syndrome (Q43753436) (← links)
- Osteochondroma of humerus in focal dermal hypoplasia (Goltz) syndrome (Q44242699) (← links)
- Goltz-Gorlin Syndrome: Revisiting the Clinical Spectrum (Q47547915) (← links)
- Oral phenotype and variation in focal dermal hypoplasia. (Q50934692) (← links)
- A nonsense porcn mutation in severe focal dermal hypoplasia with natal teeth. (Q51547821) (← links)
- Focal dermal hypoplasia: report of a case with cutaneous and skeletal manifestations. (Q52177360) (← links)
- Reticulolinear aplasia cutis congenita of the face and neck: a distinctive cutaneous manifestation in several syndromes linked to Xp22. (Q52184288) (← links)
- Focal dermal hypoplasia (Goltz syndrome) associated with intestinal malrotation and mediastinal dextroposition. (Q52202302) (← links)
- Dysmorphic disorders--an overview. (Q52220343) (← links)
- Enamel defects and Lyonization in focal dermal hypoplasia. (Q52858428) (← links)
- Focal dermal hypoplasia without focal dermal hypoplasia. (Q54414115) (← links)
- Focal dermal hypoplasia: A novel finding in disguise. (Q55405511) (← links)
- Minimal focal dermal hypoplasia in a man: A case of father-to-daughter transmission (Q67803425) (← links)
- Dental and oral lesions in two patients with focal dermal hypoplasia (Goltz syndrome) (Q73323451) (← links)
- [Focal dermal hypoplasia: description of three cases] (Q77365639) (← links)
- A Reappraisal of Eyelid Eccrine and Apocrine Hidrocystomas: Microanatomic and Immunohistochemical Studies of 40 Lesions (Q82945262) (← links)
- Epilepsy in a Patient With Focal Dermal Hypoplasia (Q83152964) (← links)