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Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene
by
Shibayama, Keiko
,
Ohyama, Yoshihide
,
Hishinuma, Akira
,
Yokota, Yukifumi
,
Kazahari, Koji
,
Kazahari, Mayumi
,
Ieiri, Tamio
,
Matsuura, Nobuo
Published in
Pediatrics international
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O13 HLA-DR, DQ genotype and heterogeneity of Japanese children with IDDM
by
Matsuura, Nobuo
,
Yokota, Fumiyuki
,
Zahari, Koujika
,
Kazahari, Mayumi
,
Oots, Nariyuki U.
,
Nomoto, Keiko
Published in
Diabetes research and clinical practice
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Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene
by
Shibayama, Keiko
,
Ohyama, Yoshihide
,
Hishinuma, Akira
,
Yokota, Yukifumi
,
Kazahari, Koji
,
Kazahari, Mayumi
,
Ieiri, Tamio
,
Matsuura, Nobuo
Published in
Pediatrics International
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Diabetes Research And Clinical Practice
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Pediatrics International
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Pediatrics International : Official Journal Of The Japan Pediatric Society
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Subclinical Hypothyroidism
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Thyrotropin Receptor Mutation
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Child
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Female
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Follow-Up Studies
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Homozygote
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Humans
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Hypothyroidism - Diagnosis
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Hypothyroidism - Genetics
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Infant, Newborn
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Life Sciences & Biomedicine
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Mutation, Missense
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Neonatal Screening
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Pediatrics
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Pediatrics, Perinatology And Child Health
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Receptors, Thyrotropin - Genetics
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Wiley-Blackwell Journals (Backfile Content)
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