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Items: 5

1.
Case report: A de novo RASopathy-causing SHOC2 variant in a Chinese girl with noonan syndrome-like with loose anagen hair
Qingming Wang, Shuangxi Cheng, Youqing Fu, Haiming Yuan
Front Genet. 2022; 13: 1040124. Published online 2022 Dec 9. doi: 10.3389/fgene.2022.1040124
PMCID:
PMC9792188
AbstractArticlePDF–1.0M
2.
Crooked fingers and sparse hair: an interesting case of trichorhinophalangeal syndrome type 1
Ramakrishna Narayanan, Srinivasa Chennareddy
BMJ Case Rep. 2015; 2015: bcr2014207645. Published online 2015 Jan 27. doi: 10.1136/bcr-2014-207645
PMCID:
PMC4322285
AbstractArticlePDF–872K
3.
Epigenetic alterations by NuRD and PRC2 in the neonatal mouse cochlea
Wanda S. Layman, Mario A. Sauceda, Jian Zuo
Hear Res. Author manuscript; available in PMC 2014 Oct 1.
Published in final edited form as: Hear Res. 2013 Oct; 304: 167–178. Published online 2013 Aug 2. doi: 10.1016/j.heares.2013.07.017
PMCID:
PMC3784354
AbstractArticlePDF–1.5M
4.
Developmental and molecular physiological evidence for the role of phosphoenolpyruvate carboxylase in rapid cotton fibre elongation
Xiao-Rong Li, Lu Wang, Yong-Ling Ruan
J Exp Bot. 2010 Jan; 61(1): 287–295. Published online 2009 Oct 8. doi: 10.1093/jxb/erp299
PMCID:
PMC2791122
AbstractArticlePDF–431K
5.
Spontaneous Mitotic Recombination and Evidence for an X-Ray-Inducible System for the Repair of DNA Damage in DROSOPHILA MELANOGASTER
James A. Kennison, Pedro Ripoll
Genetics. 1981 May; 98(1): 91–103. doi: 10.1093/genetics/98.1.91
PMCID:
PMC1214436
SummaryPDF–824K

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