While the significance of middle repetitive elements had been neglected for a long time,
there are again tendencies to ascribe most members of a given middle repetitive sequence …

Retroposition is an efficient route to move coding regions around the genome 'in search'of
novel regulatory elements and to shotgun regulatory elements into the genome 'in search'of …

Lenz microphthalmia syndrome is a rare X‐linked recessive condition first described by
Lenz in 1955 and comprises of anophthalmia, microcephaly, mental retardation, external …

Context: Dyslexia is a common disorder with a strong genetic component, but despite
significant research effort, the aetiology is still largely unknown. Objective: To identify loci …

We investigated a family with a duplication, dup (X) q26–q27, that was present in two
brothers, their mother, and their maternal grandmother. The brothers carrying the duplication …

It is now well established that genetic factors play an important role in the pathogenesis of
autism disorder and converging lines of evidence suggest the implication of the X …

BACKGROUND: A testicular germ cell tumour (TGCT) predisposing gene has been mapped
to the Xq27 region on the X chromosome. These linkage findings remain to be confirmed by …

Abstract Testicular Germ Cell Tumours (TGCT) affect 1 in 400 men in the UK. Two per cent of
TGCT cases report another affected family member. The familial relative risk is estimated to …

The term testicular cancer encompasses a group of neoplasms that occur from childhood
through to old age. This review focuses on germ-cell tumours of adolescents and adults …

A/Prof Bay Boon Huat and Prof Edward Tock for providing and help in grading the biopsies
and their concern during my study. Lecturers of the department especially A/P Yap Eu Hian …