Respiratory failure, cleft palate and epilepsy in the mouse model of human Xq22.1 deletion syndrome

Human Molecular Genetics

Volumn 23, Issue 14, 2014, Pages 3823-3829

  Zhou, Jian ^a   Goldberg, Ethan M ^b   Adrian Leu, N ^a   Zhou, Lei ^b   Coulter, Douglas A ^b   Jeremy Wang, P ^a  

^a UNIVERSITY OF PENNSYLVANIA SCHOOL OF VETERINARY MEDICINE   (United States)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE RESPIRATORY FAILURE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUDIOGENIC SEIZURE; BODY WEIGHT; CHROMOSOME DELETION; CHROMOSOME XQ; CLEFT PALATE; CONTROLLED STUDY; EMBRYO; EPILEPSY; FEMALE; GENETIC ASSOCIATION; HETEROZYGOSITY; LETHALITY; LUNG GAS EXCHANGE; MALE; MOUSE; NEWBORN; NONHUMAN; PHENOTYPE; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; RESPIRATORY FAILURE; SEIZURE; X CHROMOSOME INACTIVATION; XQ22.1 DELETION SYNDROME; ANIMAL; CHROMOSOME MAP; DISEASE MODEL; EMBRYOLOGY; GENETICS; HUMAN; LETHAL GENE; PATHOLOGY; X CHROMOSOME; X CHROMOSOME LINKED DISORDER;

ANIMALS; CHROMOSOME DELETION; CHROMOSOME MAPPING; CLEFT PALATE; DISEASE MODELS, ANIMAL; EPILEPSY; FEMALE; GENES, LETHAL; GENETIC DISEASES, X-LINKED; HUMANS; MALE; MICE; RESPIRATORY INSUFFICIENCY; X CHROMOSOME;

EID: 84902958754     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddu095     Document Type: Article

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