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Longer titles found: Incontinentia pigmenti achromians (view)

searching for incontinentia pigmenti 7 found (50 total)

alternate case: Incontinentia pigmenti

CLIC2 (689 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 -
Marion Sulzberger (251 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
PHF10 (523 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
TMLHE (971 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
Sickle cell retinopathy (2,203 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
Rhabdomyosarcoma (5,854 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 (18,861 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;