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Delineation of a region responsible for panhypopituitarism in 20p11.2
by
Dayem-Quere, Manal
,
Giuliano, Fabienne
,
Wagner-Mahler, Kathy
,
Massol, Christophe
,
Crouzet-Ozenda, Letizia
,
Lambert, Jean-Claude
,
Karmous-Benailly, Houda
Published in
American journal of medical genetics. Part A
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American Journal Of Medical Genetics Part A
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American Journal Of Medical Genetics. Part A
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20P11 Deletion
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Adolescent
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Alagille Syndrome
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Chromosome Deletion
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Chromosomes, Human, Pair 20
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Developmental Delay
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Developmental Disabilities - Genetics
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Epilepsy - Genetics
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Female
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Genetics & Heredity
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Humans
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Hypoglycemia - Genetics
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Hypopituitarism - Genetics
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In Situ Hybridization, Fluorescence
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Intellectual Disability
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Intellectual Disability - Genetics
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Life Sciences & Biomedicine
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Oligonucleotide Array Sequence Analysis
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Panhypopituitarism
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Science & Technology
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Wiley-Blackwell Journals
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