Glycosphingolipids as determinants of blood groups

TLS Online TPP Program

#Id: 2054

#Unit 8. Inheritance Biology

Leber hereditary optic neuropathy (LHON)- People who have this disorder experience rapid loss of vision in both eyes, which results from the death of cells in the optic nerve.

TLS Online TPP Program

#Id: 2073

#Unit 8. Inheritance Biology

Number of Barr bodies zero in human cells with different complements of sex chromosomes such as XO (loss of one sex chromosome) causes Turner Syndrome.

TLS Online TPP Program

#Id: 2074

#Unit 8. Inheritance Biology

Persons with Klinefelter syndrome have a Y chromosome and two or more X chromosomes in their cells such as XXY, XXYY, XXXY and XXXXY.

TLS Online TPP Program

#Id: 2075

#Unit 8. Inheritance Biology

More than two X-chromosome causes Poly-X female and Triplo-X

TLS Online TPP Program

#Id: 2076

#Unit 8. Inheritance Biology

During human chromosome rearrangements deletion onto the chromosome 5 in the short arm causes Cri-du-chat syndrome.

TLS Online TPP Program

#Id: 2077

#Unit 8. Inheritance Biology

During human chromosome rearrangements deletion onto the chromosome 4 in the short arm causes Wolf–Hirschhorn syndrome.