PCNT

См. также в других словарях:

• PCNT — Pericentrin Identifiers Symbols PCNT; KEN; MOPD2; PCN; PCNT2; PCNTB; PCTN2; SCKL4 External IDs …   Wikipedia

• PCNT — abbr. PACIFIC INTERNET LTD NASDAQ …   Dictionary of abbreviations

• Microcephalic osteodysplastic primordial dwarfism type II — Classification and external resources OMIM 210720 Microcephalic osteodysplastic primordial dwarfism type II (MOPD II) is listed as a rare disease by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that… …   Wikipedia

• Chromosome 21 (human) — Chromosome 21 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. The trisomy of the 21st chromosome causes Down Syndrome. Chromosome 21 is the smallest human chromosome, 47 million nucleotides… …   Wikipedia

• Primordial dwarfism — is a rare form of dwarfism that results in a smaller body size in all stages of life beginning from before birth. More specifically, primordial dwarfism is a diagnostic category including specific types of profoundly proportionate dwarfism, in… …   Wikipedia

• PCM1 — Pericentriolar material 1 Identifiers Symbols PCM1; PTC4 External IDs OMIM:  …   Wikipedia

• Centriole — Schematic of centriole showing microtubule triplets Three dimensi …   Wikipedia

• Marfan syndrome — Marfan redirects here. For the person after whom the syndrome is named, see Antoine Marfan. Marfan syndrome Classification and external resources Micrograph demonstrating myxomatous degeneration of the aorti …   Wikipedia

• Centrosome — Schematic of typical animal cell, showing subcellular components. Organelles: (1) Nucleolus (2) Nucleus (3) Ribosomes (little dots) (4) Vesicle (5) Rough endoplasmic reticulum (ER) (6) Golgi apparatus (7) Cytoskeleton (8) Smooth ER (9)… …   Wikipedia

• Limb-girdle muscular dystrophy — Classification and external resources ICD 10 G71.0 ICD 9 359.1 …   Wikipedia

• Hereditary spherocytosis — This article is about aspects of spherocytosis specific to the hereditary form of the disorder. For details that apply generally to this variant as well as others, see Spherocytosis. Hereditary spherocytosis Classification and external resources… …   Wikipedia