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Behavioral Differences Among Subjects With Prader-Willi Syndrome and Type I or Type II Deletion and Maternal Disomy

OBJECTIVE. To determine whether phenotypic differences exist among individuals with Prader-Willi syndrome with either type I or type II deletions of chromosome 15 or maternal disomy 15 leading to a better understanding of cause and pathophysiology of this classical genetic syndrome. METHODS. We anal...

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Bibliografiset tiedot
Julkaisussa:Pediatrics
Päätekijät: Butler, Merlin G., Bittel, Douglas C., Kibiryeva, Nataliya, Talebizadeh, Zohreh, Thompson, Travis
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2004
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6743499/
https://ncbi.nlm.nih.gov/pubmed/14993551
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1542/peds.113.3.565
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