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Polymicrogyria (PMG) is a condition that affects the development of the human brain by multiple small gyri creating excessive folding of the brain leading to an abnormally thick cortex. This abnormality can affect either one region of the brain or multiple regions.
Pituitrin is a proprietary name for an extract of bovine posterior pituitary hormones (i.e. oxytocin and vasopressin) formerly used in obstetrics and since displaced by purer preparations. [1]
22288 Ensembl ENSG00000152818 ENSMUSG00000019820 UniProt P46939 Q5T097 n/a RefSeq (mRNA) NM_007124 NM_001375323 NM_011682 RefSeq (protein) NP_009055 NP_001362252 n/a Location (UCSC) Chr 6: 144.29 – 144.85 Mb Chr 10: 12.26 – 12.75 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Utrophin is a protein that in humans is encoded by the UTRN gene. The name is a short form for ...
The term is typically applied to those whose height is not just in the upper 1% of the population but several standard deviations above mean for persons of the same sex, age, and ethnic ancestry. The term is seldom applied to those who are simply "tall" or "above average" whose heights appear to be the result of normal genetics and nutrition.
Growth hormone therapy refers to the use of growth hormone (GH) as a prescription medication—it is one form of hormone therapy.Growth hormone is a peptide hormone secreted by the pituitary gland that stimulates growth and cell reproduction.
The study of height and intelligence examines correlations between human height and human intelligence. Some epidemiological research on the subject has shown that there is a small but statistically significant positive correlation between height and intelligence after controlling for socioeconomic class and parental education. [ 1 ]
Bone morphogenetic protein 4 is a protein that in humans is encoded by BMP4 gene. [4] [5] BMP4 is found on chromosome 14q22-q23.BMP4 is a member of the bone morphogenetic protein family which is part of the transforming growth factor-beta superfamily.
Dubowitz syndrome is a rare genetic disorder characterized by microcephaly, stunted growth, and a receding chin.Symptoms vary among patients, but other characteristics include a soft, high-pitched voice, partial webbing of the fingers and toes, palate deformations, genital abnormalities, language difficulties, and an aversion to crowds. [2]
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