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Thick blood: Causes, risk factors, symptoms, and treatment

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104 Current & Future Uses of Umbilical Cord Stem Cells (Today in 2025)

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Genomic insights into prenatal diagnosis of congenital heart defects: value of CNV-seq and WES in clinical practice

- January 07, 2026

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CRISPR-Cas9 Editing of the HBG1 and HBG2 Promoters to Treat Sickle Cell Disease

- March 30, 2026

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NMC Guidelines For Competency-Based Training Programme For DM Medical Genetics

- July 18, 2025

coagulation factor deficiency syndrome :: Article Creator Factor VII Deficiency: Its Causes, Symptoms, Treatments, And More - WebMD ‌Factor VII deficiency is a rare genetic disorder. It occurs when your body can't produce enough clotting factor VII, which helps in healing wounds. It can be hereditary or be caused by an underlying medical condition. Factor VII deficiency can result in excessive bleeding due to a wound or surgery. ‌ Here is all you need to know about factor VII deficiency, along with its causes, symptoms, and treatments. ‌Your body produces 20 different clotting or coagulation factors. These are proteins that are produced by your body to heal wounds with blood clots. Factor VII, also called proconvertin, is one such clotting factor produced by the liver. It requires vitamin K for its production. Along with other clotting factors and blood cells, it promotes blood clotting at the site of an injury. It forms normal blood cl...

CRISPR-Cas9 Editing of the HBG1 and HBG2 Promoters to Treat Sickle Cell Disease

- April 05, 2026

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Solving Sickle Cell

- April 12, 2026

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Non-invasive prenatal testing: a revolutionary journey in prenatal testing

- March 06, 2026

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Non-deletional alpha thalassaemia: a review

- August 05, 2025

genetic testing for wilson's disease :: Article Creator Genetic Testing For Wilson - Search News UUHC Health Feed1y Wilson's Disease - University of Utah Health Wilson's disease is an inherited condition that causes copper to collect in your body. Wilson's disease is autosomal recessive. This means you must have two copies of the gene to develop the condition ...

Rare inherited coagulation and fibrinolytic defects that challenge diagnostic laboratories

- September 10, 2025

swyer syndrome chromosome :: Article Creator Researchers Discover Water-based Mechanism Of Human Sex Reversal At Edge Of Developmental Ambiguity Researchers from Indiana University School of Medicine have discovered a molecular "clamping" mechanism within a male-specific protein-DNA complex whose mutation causes sex reversal: children with XY chromosomes but female bodies, a condition called Swyer Syndrome. The clamp exploits a water molecule bridging the male factor (designated SRY) and DNA control sites at the tenuous beginnings of male development. The study focuses on the subtle substitution of a conserved aromatic residue in SRY (tyrosine) by a closely related aromatic residue (phenylalanine). The clinical mutation, shared by a fertile XY father and his sterile XY daughter, positions the embryonic male switch at the borderline of genetic function. The two aromatic rings are seemingly interchangeable in the structure of the protein, bu...