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Georgina Hope Rinehart (née Hancock, born 9 February 1954) is an Australian billionaire mining magnate and businesswoman. [6] She is the executive chairwoman of Hancock Prospecting, a privately owned mineral exploration and extraction company founded by her father, Lang Hancock.
16p11.2 deletion syndrome is a rare genetic condition caused by microdeletion on the short arm of chromosome 16. Most affected individuals experience global developmental delay and intellectual disability , as well as childhood-onset obesity .
Wikipedia is not a soapbox for individuals to espouse their views. However, views held by politicians, writers, and others may be summarized in their biography only to the extent those views are covered by reliable sources that are independent of the control of the politician, writer, etc.
Multiple congenital anomalies-hypotonia-seizures syndrome is a rare multi-systemic genetic disorder which is characterized by developmental delay, seizures, hypotonia and heart, urinary, and gastrointestinal abnormalities.
Interactive Forms is a mechanism to add forms to the PDF file format. PDF currently supports two different methods for integrating data and PDF forms. Both formats today coexist in the PDF specification: [38] [53] [54] [55] AcroForms (also known as Acrobat forms), introduced in the PDF 1.2 format specification and included in all later PDF ...
Smith-Kingsmore syndrome is a rare genetic disorder that is caused by gain-of-function mutation in a gene MTOR. The facial features of this syndrome are triangular face with a pointed chin, frontal bossing , hypertelorism , eyes with downslanting palpebral fissures , a flat nasal bridge , a long philtrum .
Download as PDF; Printable version; In other projects ... Peters syndrome may refer to: Peters-plus syndrome; Peters anomaly of the eye This page was last edited on ...
Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome; Microcephaly albinism digital anomalies syndrome; Mirror polydactyly-vertebral segmentation-limb defects syndrome; Morse–Rawnsley–Sargent syndrome; Multicentric carpotarsal osteolysis syndrome; Multiple congenital anomalies-hypotonia-seizures syndrome