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Genotype–phenotype correlations to aid in the prognosis of individuals with uncommon 20q13.33 subtelomere deletions: a collaborative study on behalf of the ‘association des Cytogénéticiens de langue Française’.
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- European Journal of Human Genetics, 2007, v. 15, n. 4, p. 446, doi. 10.1038/sj.ejhg.5201784
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- Article
Additional evidence to support the role of the 20q13.33 region in susceptibility to autism.
- Published in:
- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 6, p. 1505, doi. 10.1002/ajmg.a.35878
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- Publication type:
- Article