| P50 | author | Dwight Stambolian | Q65038293 |
| P2093 | author name string | Jack Favor | |
| | Ken S. Wang | |
| | Kristen M. Huang | |
| | Lauren E. Zahn | |
| P2860 | cites work | The recessive phenotype displayed by a dominant negative microphthalmia-associated transcription factor mutant is a result of impaired nucleation potential | Q36557590 |
| | Asymmetrical retinoic acid synthesis in the dorsoventral axis of the retina | Q41621708 |
| | Visual cycle impairment in cellular retinaldehyde binding protein (CRALBP) knockout mice results in delayed dark adaptation | Q43574293 |
| | Dominant cataract and recessive specific locus mutations in offspring of X-irradiated male mice | Q44771660 |
| | Gene expression of growth and differentiation factors-5, -6, and -7 in developing bovine tooth at the root forming stage | Q48039406 |
| | EGF and TGF-alpha stimulate retinal neuroepithelial cell proliferation in vitro | Q48717073 |
| | Novel mutation in sonic hedgehog in non-syndromic colobomatous microphthalmia. | Q51951452 |
| | Mouse Otx2 functions in the formation and patterning of rostral head. | Q52205211 |
| | Changing Patterns of the Retinoic Acid System in the Developing Retina | Q60439770 |
| | Zebrafish Radar: a new member of the TGF-beta superfamily defines dorsal regions of the neural plate and the embryonic retina | Q72201867 |
| | Screening for PAX6 gene mutations is consistent with haploinsufficiency as the main mechanism leading to various ocular defects | Q73121121 |
| | Genetic mapping of a mouse ocular malformation locus, Tcm, to chromosome 4 | Q73152894 |
| | Dosage requirement and allelic expression of PAX6 during lens placode formation | Q73186161 |
| | Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. Percin EF, Ploder LA, Yu JJ, Arici K, Horsford DJ, Rutherford A, Bapat B, Cox DW, Duncan AMV, Kalnins VI, Kocak-Altintas A, Sowden JC, Trabousli E, Sarfarazi M, McInn | Q73849259 |
| | Otx genes are required for tissue specification in the developing eye | Q74330538 |
| | Mutations in a new member of the chromodomain gene family cause CHARGE syndrome | Q24300737 |
| | Characterization of the CHD family of proteins | Q24317090 |
| | Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosa | Q24317582 |
| | Basic local alignment search tool | Q25938991 |
| | Xenopus GDF6, a new antagonist of noggin and a partner of BMPs | Q28138690 |
| | Recessive mutations in the RLBP1 gene encoding cellular retinaldehyde-binding protein in a form of retinitis punctata albescens | Q28140235 |
| | Aspartyl beta -hydroxylase (Asph) and an evolutionarily conserved isoform of Asph missing the catalytic domain share exons with junctin | Q28144446 |
| | Ocular phenotype of bothnia dystrophy, an autosomal recessive retinitis pigmentosa associated with an R234W mutation in the RLBP1 gene | Q28200079 |
| | Ligand specificity in the CRAL-TRIO protein family | Q28206484 |
| | Multiple joint and skeletal patterning defects caused by single and double mutations in the mouse Gdf6 and Gdf5 genes | Q28212192 |
| | Molecular cloning and structural analysis of the human gene encoding cellular retinaldehyde-binding protein | Q28238920 |
| | PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects | Q28240060 |
| | Limb alterations in brachypodism mice due to mutations in a new member of the TGF beta-superfamily | Q28251546 |
| | Absence of post-translational aspartyl beta-hydroxylation of epidermal growth factor domains in mice leads to developmental defects and an increased incidence of intestinal neoplasia | Q28509997 |
| | Mutually regulated expression of Pax6 and Six3 and its implications for the Pax6 haploinsufficient lens phenotype | Q28586457 |
| | Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation | Q28589610 |
| | Lhx2, a LIM homeobox gene, is required for eye, forebrain, and definitive erythrocyte development | Q28591652 |
| | Mouse small eye results from mutations in a paired-like homeobox-containing gene | Q29617930 |
| | Map Manager QTX, cross-platform software for genetic mapping | Q31030142 |
| | The control of cell fate in the embryonic visual system by atonal, tailless and EGFR signaling. | Q33178488 |
| | CHD5, a new member of the chromodomain gene family, is preferentially expressed in the nervous system | Q34178216 |
| | Mutations in SOX2 cause anophthalmia | Q34180637 |
| | Mutations in the human RAX homeobox gene in a patient with anophthalmia and sclerocornea | Q34282029 |
| | The Rx homeobox gene is essential for vertebrate eye development | Q34428244 |
| | Genomic, transcriptional and mutational analysis of the mouse microphthalmia locus | Q34609365 |
| | PAX6 in sensory development | Q34641592 |
| | Retinoic acid is necessary for development of the ventral retina in zebrafish. | Q35626548 |
| P433 | issue | 5 | |
| P921 | main subject | Mitofusin 2 | Q15334427 |
| P304 | page(s) | 332–343 | |
| P577 | publication date | 2005-05-01 | |
| P1433 | published in | Mammalian Genome | Q1348949 |
| P1476 | title | Genetic and phenotypic analysis of Tcm, a mutation affecting early eye development | |
| P478 | volume | 16 | |