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Author/Creator Bober, Michael B.

1. A multicenter study to evaluate pulmonary function in osteogenesis imperfecta. Issue 6 (24th September 2018)

Authors:
Tam, Allison; Chen, Shan; Schauer, Evan; Grafe, Ingo; Bandi, Venkata; Shapiro, Jay R.; Steiner, Robert D.; Smith, Peter A.; Bober, Michael B.; Hart, Tracy; Cuthbertson, David; Krischer, Jeffrey; Mullins, Mary; Byers, Peter H.; Sandhaus, Robert A.; Durigova, Michaela; Glorieux, Francis H.; Rauch, ...
Journal:
Clinical genetics
Issue:
Volume 94:Issue 6(2018)
Page Start:
502
Record Type:
Journal Article
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4. Aneurysmal bone cysts and pathologic fracture associated with supernumerary ring chromosome 6 in two unrelated patients. Issue 12 (28th October 2017)

Authors:
Hurd, Lauren M.; Thacker, Mihir M.; Okenfuss, Ericka; Duker, Angela L.; Lou, Yang; Harty, Mary P.; Conard, Katrina; Lian, Jane B.; Bober, Michael B.
Journal:
American journal of medical genetics
Issue:
Volume 173:Issue 12(2017)
Page Start:
3205
Record Type:
Journal Article
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6. Best practices in peri‐operative management of patients with skeletal dysplasias. Issue 10 (1st August 2017)

Authors:
White, Klane K.; Bompadre, Viviana; Goldberg, Michael J.; Bober, Michael B.; Cho, Tae‐Joon; Hoover‐Fong, Julie E.; Irving, Melita; Mackenzie, William G.; Kamps, Shawn E.; Raggio, Cathleen; Redding, Gregory J.; Spencer, Samantha S.; Savarirayan, Ravi; Theroux, Mary C.
Journal:
American journal of medical genetics
Issue:
Volume 173:Issue 10(2017)
Page Start:
2584
Record Type:
Journal Article
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7. Best practices in the evaluation and treatment of foramen magnum stenosis in achondroplasia during infancy. Issue 1 (23rd September 2015)

Authors:
White, Klane K.; Bompadre, Viviana; Goldberg, Michael J.; Bober, Michael B.; Campbell, Jeffrey W.; Cho, Tae‐Joon; Hoover‐Fong, Julie; Mackenzie, William; Parnell, Shawn E.; Raggio, Cathleen; Rapoport, David M.; Spencer, Samantha A.; Savarirayan, Ravi
Journal:
American journal of medical genetics
Issue:
Volume 170:Issue 1(2016)
Page Start:
42
Record Type:
Journal Article
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8. Biallelic variants in DNA2 cause microcephalic primordial dwarfism. Issue 8 (23rd June 2019)

Authors:
Tarnauskaitė, Žygimantė; Bicknell, Louise S.; Marsh, Joseph A.; Murray, Jennie E.; Parry, David A.; Logan, Clare V.; Bober, Michael B.; de Silva, Deepthi C.; Duker, Angela L.; Sillence, David; Wise, Carol; Jackson, Andrew P.; Murina, Olga; Reijns, Martin A. M.
Journal:
Human mutation
Issue:
Volume 40:Issue 8(2019)
Page Start:
1063
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗