Origin
It was only in 1943, when two parents named Julia Bell and J. Purdon Martin discovered a syndrome now known as Fragile X Syndrome. This syndrome is also known as Martin-Bell syndrome, marker X syndrome or Fragile X. It is the most common cause of inherited mental retardation and is the second most common cause of genetically associated mental deficiencies after trisomy 21. They discovered this syndrome when 11 of their family members had this condition.
In 1969 was when scientist Herbert Lubs discovered the real identity of Fragile X a by and made it a world wide known genetic disorder. He discovered that you get fragile X by one of the genes changing in the X chromsome hence the name Fragile X Syndrome.
It was only in 1943, when two parents named Julia Bell and J. Purdon Martin discovered a syndrome now known as Fragile X Syndrome. This syndrome is also known as Martin-Bell syndrome, marker X syndrome or Fragile X. It is the most common cause of inherited mental retardation and is the second most common cause of genetically associated mental deficiencies after trisomy 21. They discovered this syndrome when 11 of their family members had this condition.
In 1969 was when scientist Herbert Lubs discovered the real identity of Fragile X a by and made it a world wide known genetic disorder. He discovered that you get fragile X by one of the genes changing in the X chromsome hence the name Fragile X Syndrome.