Author/Creator: Cheung, Moira S. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Cheung, Moira S.

1. Automated reanalysis, a novel way to diagnose an ultra-rare condition: Fibronectin-1-related spondylometaphyseal dysplasia (SMD-FN1). Issue 3 (17th February 2021)

Authors:: Sabir, Ataf H.; Singhal, Juhi; Man, Jessica; Mensah, Nana Ekuntan; Ahn, Joo Wook; Cheung, Moira S.; Irving, Melita
Journal:: Clinical dysmorphology
Issue:: Volume 30:Issue 3(2021)
Page Start:: 154
Record Type:: Journal Article
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2. Automated reanalysis, a novel way to diagnose an ultra-rare condition: Fibronectin-1-related spondylometaphyseal dysplasia (SMD-FN1). Issue 3 (July 2021)

Authors:: Sabir, Ataf H.; Singhal, Juhi; Man, Jessica; Mensah, Nana Ekuntan; Ahn, Joo Wook; Cheung, Moira S.; Irving, Melita
Journal:: Clinical dysmorphology
Issue:: Volume 30:Issue 3(2021)
Page Start:
Record Type:: Journal Article
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3. Earlier detection of hypochondroplasia: A large single‐center UK case series and systematic review. Issue 1 (14th October 2020)

Authors:: Sabir, Ataf H.; Sheikh, Jameela; Singh, Ananya; Morley, Elizabeth; Cocca, Alessandra; Cheung, Moira S.; Irving, Melita
Journal:: American journal of medical genetics
Issue:: Volume 185:Issue 1(2021)
Page Start:: 73
Record Type:: Journal Article
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4. Management of primary and secondary osteoporosis in children. (October 2020)

Authors:: Sakka, Sophia D.; Cheung, Moira S.
Journal:: Therapeutic advances in musculoskeletal disease
Issue:: Volume 12(2020)
Page Start:
Record Type:: Journal Article
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