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Longer titles found: Incontinentia pigmenti achromians (view)

searching for Incontinentia pigmenti 9 found (55 total)

alternate case: incontinentia pigmenti

CLIC2 (703 words) [view diff] exact match in snippet view article find links to article

tissue. This gene maps to the candidate region on chromosome X for incontinentia pigmenti. Chloride channel GRCh38: Ensembl release 89: ENSG00000155962 –
PHF10 (524 words) [view diff] exact match in snippet view article find links to article
(October 1996). "Transcriptional analysis of the candidate region for incontinentia pigmenti (IP2) in Xq28". Genome Research. 6 (10): 922–34. doi:10.1101/gr
Marion Sulzberger (253 words) [view diff] exact match in snippet view article find links to article
Sulzberger MB. Ueber eine bisher nicht beschriebene Pigmentaffektion (Incontinentia pigmenti). Arch Dermatol Syph (Berlin) 1928; 154: 19–32 Geiges, Michael L
TMLHE (975 words) [view diff] exact match in snippet view article find links to article
(October 1996). "Transcriptional analysis of the candidate region for incontinentia pigmenti (IP2) in Xq28". Genome Research. 6 (10): 922–34. doi:10.1101/gr
Action Medical Research (1,143 words) [view diff] exact match in snippet view article find links to article
of cleft lip and palate, and for the hereditary skin condition incontinentia pigmenti – which causes severe blistering of the skin. Discovering the genes
Sickle cell retinopathy (2,209 words) [view diff] exact match in snippet view article find links to article
Radiation retinopathy Retinopathy of prematurity Unclassified causes Incontinentia pigmenti Autosomal dominant vitreoretinochoroidopathy Chronic rhegmatogenous
Hypohidrotic ectodermal dysplasia with immune deficiency (2,212 words) [view diff] exact match in snippet view article find links to article
deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)". American Journal of Human
Rhabdomyosarcoma (5,957 words) [view diff] exact match in snippet view article find links to article
familial atypical multiple mole melanoma syndrome, hereditary tylosis, incontinentia pigmenti, and supernumerary nipples". Dermatologic Clinics. 13 (1): 211–229
List of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article
recessive; 600737; GNE Inclusion body myopathy-3; 605637; MYH2 Incontinentia pigmenti, type II; 308300; IKBKG Infantile neuroaxonal dystrophy 1; 256600;