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A male infant with Xq22.2q22.3 duplication containing PLP1 and MID2
by
Chanchani, Swati R.
,
Xie, Hongyan
,
Sekhon, Gurbax
,
Melikishvili, Ana M.
,
Moyer Harasink, Sue
,
Pall, Harpreet
,
Giampietro, Philip F.
Published in
Molecular genetics & genomic medicine
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Molecular Genetics & Genomic Medicine
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Bladder
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Chromosom
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Chromosome Duplication
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Chromosomes
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Chromosomes, Human, X - Genetics
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Craniofacial Abnormalities - Genetics
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Disease Control
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Family Medical History
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Fetal Growth Retardation - Genetics
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Fetal Growth Retardation - Pathology
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Fg Syndrome
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Fluorescence
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Fluorescence In Situ Hybridization
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Fluoreszenz
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