CrossRef Text and Data Mining
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Haddad Syndrome with a Germ-Line Mutation in the PHOX2B Gene in a Korean Neonate.
Chunglyul Baek, Ji Mi Jung, Yun Jung Lim, Ki Hoon Kim, Han Wook Yu, Gu Hwan Kim, Mi Lim Chung
Neonatal Med. 2015;22(3):162-167.   Published online August 31, 2015

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Haddad Syndrome with a Germ-Line Mutation in thePHOX2BGene in a Korean Neonate
Neonatal Medicine. 2015;22(3):162   Crossref logo

A Case of Congenital Central Hypoventilation Syndrome with PHOX2B Gene Mutation in a Korean Neonate
Journal of Korean Medical Science. 2010;25(8):1237   Crossref logo
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Homozygous mutation of the PHOX2B gene in congenital central hypoventilation syndrome (Ondine's Curse)
Human Mutation. 2008;29(5):770-770   Crossref logo
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Concomitant existence of total bowel aganglionosis and congenital central hypoventilation syndrome in a neonate with PHOX2B gene mutation
Journal of Pediatric Surgery. 2007;42(2):e9-e11   Crossref logo
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Gorlin syndrome: Identification of 4 novel germ-line mutations of the human patched (PTCH) gene
Human Mutation. 1998;11(6):480-480   Crossref logo
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Congenital Central Hypoventilation Syndrome with PHOX2B Gene Mutation
The Indian Journal of Pediatrics. 2012;79(11):1526-1528   Crossref logo
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Germ-line transmission of a c-abl mutation produced by targeted gene disruption in ES cells
Trends in Genetics. 1990;6:6   Crossref logo
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Probable involvement of a germ-line mutation of an unknown mismatch repair gene in a Japanese Muir-Torre syndrome phenotype
Journal of Dermatological Science. 2000;23(2):117-125   Crossref logo
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Identification of a novel TGFBR2 gene mutation in a Korean patient with Loeys-Dietz aortic aneurysm syndrome; no mutation in TGFBR2 gene in 30 patients with classic Marfan's syndrome
Clinical Genetics. 2005;68(6):561-563   Crossref logo
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Is Mitochondrial Donation Germ-Line Gene Therapy? Classifications and Ethical Implications
Bioethics. 2016;31(1):55-67   Crossref logo
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