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Langer-Giedion Syndrome Websites

Langer-Giedion syndrome is a rare autosomal dominant genetic disorder caused by a deletion of chromosomal material. Associated features include learning difficulties, short stature, distinctive facial features, small head and skeletal abnormalities- Category ID : 75929
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Indian Pediatrics: Langer-Giedion Syndrome

Provides clinical information on this disorder including the case study of a 12 year old girl.
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Genetics Home Reference: Langer-Giedion Syndrome

Provides information on this condition, the genetic changes involved, how it is inherited and other sources of information.
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Trichorhinophalangeal Syndrome Type II; TRPS2

Technical information on this disorder, also known as Langer-Giedion syndrome, from the database of Online Mendelian Inheritance in Man.
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