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Karyotype Of Prader-Willi Syndrome, Labelled 3D Illustration. A Genetic Disorder Caused By A Lack Of Function Of Part Of Chromosome 15 Inherited From A Person'S Father

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Karyotype of Prader-Willi syndrome, labelled 3D illustration. A genetic disorder caused by a lack of function of part of chromosome 15 inherited from a person's father

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KEYWORDS

angelman syndrome karyotype 15 chromosome partial deletion dna biology genetics 3d illustration gene science human medical evolution genetic macro research health white background microbiology cell structure genome medicine mutation biochemistry reproduction molecule microscope render healthcare isolated female male disorder long arm lower father labelled paternal

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Karyotype of Prader-Willi syndrome
Karyotype of Prader-Willi syndrome
Karyotype of Prader-Willi syndrome
Karyotype of Prader-Willi syndrome
Karyotype of Prader-Willi syndrome

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