microphthalmia - Robuta Search

https://www.semanticscholar.org/topic/Microphthalmia%2C-Syndromic-3/6751713 Microphthalmia, Syndromic 3 | Semantic Scholar semantic scholar https://rarediseases.info.nih.gov/diseases/17575/colobomatous-microphthalmia-obesity-hypogenitalism-intellectual-disability-syndrome Colobomatous microphthalmia - obesity - hypogenitalism - intellectual disability syndrome | About... Find symptoms and other information about Colobomatous microphthalmia - obesity - hypogenitalism - intellectual disability syndrome. intellectual disability obesity syndrome https://pubmed.ncbi.nlm.nih.gov/20688706/ Bilateral complex microphthalmia with intraocular dermoid cyst in a neonate red deer (Cervus... A 3-day-old, male red deer (Cervus elaphus) with bilateral microphthalmia was found dead in the Western Alps in northern Italy. No other gross alterations were... https://www.semanticscholar.org/topic/microphthalmia-associated-transcription-factor/181659 microphthalmia-associated transcription factor | Semantic Scholar A basic helix-loop-helix leucine zipper transcription factor that regulates the CELL DIFFERENTIATION and development of a variety of cell types including... transcription factor associated semantic scholar https://www.scirp.org/journal/paperinformation?paperid=5501 Expression of Microphthalmia Transcription Factor in Sentinel Lymph Nodes of Patients with Melanoma Background: Sentinel lymph node biopsy is widely used in the management of melanoma patients. Multiple markers are used to stain sentinel lymph node tissue... transcription factor https://disorders.eyes.arizona.edu/disorders/coloboma-microphthalmia-albinism-and-deafness Coloboma, Microphthalmia, Albinism, and Deafness | Hereditary Ocular Diseases coloboma albinism deafness hereditary ocular https://www.ncbi.nlm.nih.gov/medgen/C3150968 Microphthalmia, isolated, with coloboma 6 (Concept Id: C3150968) - MedGen - NCBI isolated coloboma concept id medgen https://pubmed.ncbi.nlm.nih.gov/18950397/ Microphthalmia with linear skin defects: a case report and review Microphthalmia with linear skin defects syndrome is an X-linked dominant disorder characterized by microphthalmia and other ocular anomalies as well as linear,... a case linear skin defects report https://infoscience.epfl.ch/entities/publication/660cce36-e997-4f54-b0ad-dd4a342619ae Ectopic expression of RET results in microphthalmia and tumors in the retinal pigment epithelium The retinal pigment epithelium (RPE) is essential for eye development by interacting with the overlaying neuroepithelium. Regulatory sequences of the gene... https://disorders.eyes.arizona.edu/references/de-novo-mutations-smchd1-cause-bosma-arhinia-microphthalmia-syndrome-and-abrogate-nasal De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal... https://rarediseases.info.nih.gov/diseases/12640/frontonasal-dysplasia-severe-microphthalmia-severe-facial-clefting-syndrome Frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome | About the Disease... Find symptoms and other information about Frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome. about the dysplasia severe facial syndrome https://profiles.wustl.edu/en/publications/the-melanocyte-specific-isoform-of-the-microphthalmia-transcripti/fingerprints/?sortBy=alphabetically The melanocyte-specific isoform of the microphthalmia transcription factor affects the phenotype of... transcription factor melanocyte specific isoform affects https://www.wikidata.org/wiki/Q59096765 MAP kinase links the transcription factor Microphthalmia to c-Kit signalling in melanocytes -... scientific article published on January 15, 1998 https://disorders.eyes.arizona.edu/references/hereditary-cataracts-and-microphthalmia HEREDITARY CATARACTS AND MICROPHTHALMIA | Hereditary Ocular Diseases hereditary cataracts ocular diseases