Journal of Clinical Genomics is a transdisciplinary, peer reviewed journal that aims to publish original research papers on #Molecular_biology & #Genetics.
An unusual condition characterized by pyramidal molar roots and #taurodontism, associated with complex anomalies. This has been identified in two generations of the same family. Both the parents and their six sibs had pyramidal, taurodontal or molar origins.
Grebe #chondrodysplasia is an autosomal recessive disorder characterized by a severe abnormality of limb and limb joints. The severity of the limb shortening progresses in the proximal-distal gradient, with the most affected hands and feet.
#Pachygyria is a cerebral hemisphere congenital malformation. It results in the cerebral cortex having unusually thick convolutions. Children usually have developmental delays and seizures, depending on the severity of the cortical malformation, the onset, and severity.
Human beings are especially vulnerable to developing advanced #carcinomas in the form of tumors that include prostate, breast, lung, and colorectal cancers in comparison with chimpanzees.
An unusual condition characterized by pyramidal molar roots and #taurodontism, associated with complex anomalies. This has been identified in two generations of the same family. Both the parents and their six sibs had pyramidal, taurodontal or molar origins.
The disease of #Saethre_Chotzen is an inherited disorder caused by premature fusion of the bones of the skull (craniosynostosis). This early fusion prevents the normal development of the brain and affects the head and face.
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#Adult_onset_immunodeficiency with anti-interferon-gamma autoantibodies is a condition of immunodeficiency. It is associated with the propensity to transmit infections caused by microbes that usually affect only persons with poor immune systems.
Drinking plenty of both green tea and coffee among individuals with type 2 #diabetes is linked to a lower risk of dying from either cause, new research suggests.
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#Sideroblastic_pyridoxine-refractory autosomal recessive anemia is an inherited blood condition characterized by bone marrow's compromised capacity to manufacture normal red blood cells.
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#Autoimmune_hemolytic anemia is a rare condition in red blood cells, and an immune deficiency. When the body produces antibodies to kill the red blood cells, it happens. Hemolytic anemia occurs when not enough red blood cells are present.
An unusual condition characterized by pyramidal molar roots and #taurodontism, associated with complex anomalies. This has been identified in two generations of the same family. Both the parents and their six sibs had pyramidal, taurodontal, or molar origins.
#Pachygyria is a cerebral hemisphere congenital malformation. It results in the cerebral cortex having unusually thick convolutions. Children usually have developmental delays and seizures, depending on the severity of the cortical malformation, the onset, and severity.
#Methylmalonic_acidemia is a condition in which the body is unable to break down certain proteins and fats. The result is the build-up of a substance in the blood called methylmalonic acid. It is one of several conditions called a "inborn metabolism error."
The disease of #Saethre_Chotzen is an inherited disorder caused by premature fusion of the bones of the skull (craniosynostosis). This early fusion prevents normal development of the brain and affects the head and face form.
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#Sideroblastic_pyridoxine-refractory autosomal recessive anemia is an inherited blood condition characterized by bone marrow's compromised capacity to manufacture normal red blood cells.
Submit your submission here: https://t.co/nMiZVi5cyf
#Cholecystitis is an inflammation of the gallbladder. Your gallbladder is a small, pear-shaped organ on the right side of your abdomen, under your liver.
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The disease of #Saethre_Chotzen is an inherited disorder caused by premature fusion of the bones of the skull (craniosynostosis). This early fusion prevents the normal development of the brain and affects the head and face.
Share your views Email us: [email protected]
#Hereditary_spastic_paraplegia (HSP) is a category of inherited disorders characterized by progressive weakness and spasticity (stiffness) of the legs, also called family spastic paraparesis (FSP). Early in the course of the disease, gait problems and stiffness can be mild.
An unusual condition characterized by pyramidal molar roots and #taurodontism, associated with complex anomalies. This has been identified in two generations of the same family. Both the parents and their six sibs had pyramidal, taurodontal, or molar origins.
The disease of #Saethre_Chotzen is an inherited disorder caused by premature fusion of the bones of the skull (craniosynostosis). This early fusion prevents the normal development of the brain and affects the head and face.
Share your views Email us: [email protected]