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  • Health - 30 Dec 2022
    Kallmann syndrome is a medical condition marked by the delayed onset or absence of puberty, along with an impaired or absent sense of smell, known as hyposmia or anosmia respectively. It is a type of...
  • Health - 30 Dec 2022
    Albinism is a condition marked by reduced production of melanin, the pigment that provides color to the hair, skin, and eyes of an individual. It is an inherited condition with the signs present from...
  • Health - 30 Dec 2022
    Interrupted aortic arch is a rare congenital heart condition first describedby Steidele in 1773. The condition accounts for less than 1% of congenital heart conditions and is part of a broader...
  • Health - 29 Dec 2022
    Assisted reproductive techniques (ART) took a quantum leap in 1978 with the birth of the first ‘test-tube baby,’ Louise Brown, who was conceived through in vitro fertilization (IVF), crowning decades...
  • Health - 29 Dec 2022
    The NIPT (noninvasive prenatal testing) is a genetic test performed on pregnant women, in order to detect fetal chromosomal aneuploidies. It is based upon the testing of cell-free fetal DNA (cf-fDNA)...
  • Health - 9 Dec 2022
    Diabetes mellitus (DM) is a group of metabolic disorders that cause sustained high blood sugar levels. In the past, only two types of diabetes were known, type 1 and type 2.
  • Health - 8 Nov 2022
    Hypophosphatasia is an inherited metabolic disorder that affects the bones and teeth.
  • White Paper - 3 Nov 2022
    This article looks at moving beyond LIMS for forensic investigation.
  • Health - 6 Sep 2022
    The term hypoxia is a condition where the tissues are not oxygenated adequately, usually due to an insufficient concentration of oxygen in the blood.
  • Health - 11 Jul 2022
    Binder syndrome, also known as nasomaxillary dysplasia or maxillo-nasal dysostosis, is a rare congenital condition causing developmental defects.

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