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Author/Creator Allen, William

4. Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders. Issue 17 (27th May 2021)

Authors:
Reis, Linda M; Sorokina, Elena A; Dudakova, Lubica; Moravikova, Jana; Skalicka, Pavlina; Malinka, Frantisek; Seese, Sarah E; Thompson, Samuel; Bardakjian, Tanya; Capasso, Jenina; Allen, William; Glaser, Tom; Levin, Alex V; Schneider, Adele; Khan, Ayesha; Liskova, Petra; Semina, Elena V
Journal:
Human molecular genetics
Issue:
Volume 30:Issue 17(2021)
Page Start:
1591
Record Type:
Journal Article
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5. Cover Image, Volume 176A, Number 4, April 2018. Issue 4 (25th March 2018)

Authors:
Zarate, Yuri A.; Smith‐Hicks, Constance L.; Greene, Carol; Abbott, Mary‐Alice; Siu, Victoria M.; Calhoun, Amy R. U. L.; Pandya, Arti; Li, Chumei; Sellars, Elizabeth A.; Kaylor, Julie; Bosanko, Katherine; Kalsner, Louisa; Basinger, Alice; Slavotinek, Anne M.; Perry, Hazel; Saenz, Margarita; Szybow...
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 4(2018)
Page Start:
n/a
Record Type:
Journal Article
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7. Dysregulations of sonic hedgehog signaling in MED12‐related X‐linked intellectual disability disorders. Issue 4 (6th February 2019)

Authors:
Srivastava, Siddharth; Niranjan, Tejasvi; May, Melanie M.; Tarpey, Patrick; Allen, William; Hackett, Anna; Jouk, Pierre‐Simon; Raymond, Lucy; Briault, Slyvain; Skinner, Cindy; Toutain, Annick; Gecz, Jozef; Heath, William; Stevenson, Roger E.; Schwartz, Charles E.; Wang, Tao
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 7:Issue 4(2019)
Page Start:
n/a
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗