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Baller-Gerold Syndrome in a Premature Infant with a Mutation in the RECQL4 Gene
Ji Sook Kim
Neonatal Med. 2019;26(4):240-245.   Published online November 29, 2019
DOI: https://doi.org/10.5385/nm.2019.26.4.240

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Baller-Gerold Syndrome in a Premature Infant with a Mutation in the RECQL4 Gene
Neonatal Medicine. 2019;26(4):240-245   Crossref logo
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The molecular role of the Rothmund-Thomson-, RAPADILINO- and Baller-Gerold-gene product, RECQL4: recent progress
Cellular and Molecular Life Sciences. 2007;64(7-8):796-802   Crossref logo
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Baller-Gerold syndrome Craniosynostosis-radial aplasia syndrome
Clinical Genetics. 2008;17(2):161-166   Crossref logo
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TWIST gene mutation in a patient with radial aplasia and craniosynostosis: Further evidence for heterogeneity of Baller-Gerold syndrome
American Journal of Medical Genetics. 1999;82(2):170-176   Crossref logo
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SFTPC gene mutation p.R167Q in a premature infant
Pediatric Pulmonology. 2013;49(3):E66-E68   Crossref logo
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Baller - Gerold syndrome
The Indian Journal of Pediatrics. 2002;69(12):1097-1098   Crossref logo
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Is there a Baller-Gerold syndrome?
American Journal of Medical Genetics. 1996;61(1):63-64   Crossref logo
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Baller-Gerold Syndrome a Rare Cause of Heart-Hand Syndrome
ISRN Cardiology. 2011;2011:1-3   Crossref logo
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Baller-Gerold syndrome: A postmortem examination
American Journal of Medical Genetics. 1993;47(8):1233-1233   Crossref logo
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Baller Gerold syndrome and Fanconi anaemia
American Journal of Medical Genetics. 1998;75(2):228-229   Crossref logo
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