Results 1 -
10
of
24
for
Not genetically inherited
- ... of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome. Kidney Int. 2006 Sep;70(6):1155-69. doi: 10.1038/sj.ki.5001728. Epub 2006 Aug 2. Citation on PubMed
- ... in some affected individuals. ... signs and symptoms of the condition. Individuals who are genetically male and have two copies of a mutated ...
- ... sex characteristics during puberty. ... of the condition. Although people who are genetically female (with two X chromosomes in each cell) ...
- ... Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndrome. Blood. 2010 Jun 24; ...
- ... milder signs and symptoms. ... have mutations in both copies of the LHCGR gene and are genetically male (with one X and one Y chromosome ...
- ... worldwide. The condition is more common in certain genetically isolated populations: 1 in 75 in a small ... called pseudoarylsulfatase deficiency. ARSA PSAP This condition is inherited in an autosomal recessive pattern, which means both ...
- ... and breathing problems.Infants with SIDDT who are genetically male, with one X chromosome and one Y ... or clearly female. In affected infants who are genetically female, with two X chromosomes in each cell, ...
- ... Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome. Trends Genet. 2008 ...
- ... 1002/ajh.21313. Citation on PubMed Percy MJ. Genetically heterogeneous origins of idiopathic erythrocytosis. Hematology. 2007 Apr; ...
- ... Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease. J Med Genet. 2011 Oct; ...