Deletion Syndrome

Some articles on deletion syndrome, deletion, deletions, syndrome:

Chromosome 22 (human) - Chromosomal Conditions
... or number of copies of chromosome 22 22q11.2 deletion syndrome Most people with 22q11.2 deletion syndrome are missing about 3 million base pairs on one copy of chromosome 22 in each cell ... The deletion occurs near the middle of the chromosome at a location designated as q11.2 ... A small percentage of affected individuals have shorter deletions in the same region ...
Trisomy 22
... Emanuel Syndrome is named after the genetic contributions made by researcher Dr. 22q11 Deletion Syndrome is a rare condition which occurs in approximately 1 in 4000 births ... This condition has several different names, The 22q11.2 Deletion Sydrome, Velocardiofacial syndrome, DiGeorge Syndrome, Conotruncal Anomaly Face syndrome, Opitz G/BBB Syndrome, Cayler Cardiofacial ...
List Of Diseases (0-9) - 1–3
... dehydrogenase deficiency, rare (NIH) 17q21.31 microdeletion syndrome 18-Hydroxylase deficiency, rare (NIH) 18p deletion syndrome 1p36 Deletion Syndrome, rare (NIH) 2-hydroxyet ...
Tetrasomy - Causes - Sex-chromosome Tetrasomies
48, XXXX syndrome 48, XXYY syndrome Klinefelter's syndrome, where XXXY tetrasomy is present Pathology chromosome abnormalities (Q90–Q99, 758) Autosomal Trisomies Down syndrome 21 ...

Famous quotes containing the word syndrome:

    [T]he syndrome known as life is too diffuse to admit of palliation. For every symptom that is eased, another is made worse. The horse leech’s daughter is a closed system. Her quantum of wantum cannot vary.
    Samuel Beckett (1906–1989)