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Author/Creator Williams, Linford

1. De novo missense variants in MEIS2 recapitulate the microdeletion phenotype of cardiac and palate abnormalities, developmental delay, intellectual disability and dysmorphic features. Issue 9 (28th July 2018)

Authors:
Douglas, Ganka; Cho, Megan T.; Telegrafi, Aida; Winter, Susan; Carmichael, Jason; Zackai, Elaine H.; Deardorff, Matthew A.; Harr, Margaret; Williams, Linford; Psychogios, Apostolos; Erwin, Angelika L.; Grebe, Theresa; Retterer, Kyle; Juusola, Jane
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 9(2018)
Page Start:
1845
Record Type:
Journal Article
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3. Phenotypic expansion of Bosch–Boonstra–Schaaf optic atrophy syndrome and further evidence for genotype–phenotype correlations. Issue 6 (10th April 2020)

Authors:
Rech, Megan E.; McCarthy, John M.; Chen, Chun‐An; Edmond, Jane C.; Shah, Veeral S.; Bosch, Daniëlle G. M.; Berry, Gerard T.; Williams, Linford; Madan‐Khetarpal, Suneeta; Niyazov, Dmitriy; Shaw‐Smith, Charles; Kovar, Erin M.; Lupo, Philip J.; Schaaf, Christian P.
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 6(2020)
Page Start:
1426
Record Type:
Journal Article
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4. Suppression of autophagy by FIP200 deletion leads to osteopenia in mice through the inhibition of osteoblast terminal differentiation. (18th October 2013)

Authors:
Liu, Fei; Fang, Fang; Yuan, Hebao; Yang, Dongye; Chen, Yongqiang; Williams, Linford; Goldstein, Steven A; Krebsbach, Paul H; Guan, Jun‐Lin
Journal:
Journal of bone and mineral research
Issue:
Volume 28:Number 11(2013:Nov.)
Page Start:
2414
Record Type:
Journal Article
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