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Deletions in chromosome 2 and fragile sites.
Palmer CG, Heerema N, Bull M. Palmer CG, et al. Among authors: bull m. Am J Med Genet. 1990 Jun;36(2):214-8. doi: 10.1002/ajmg.1320360215. Am J Med Genet. 1990. PMID: 2368809
Novel PLS3 variants in X-linked osteoporosis: Exploring bone material properties.
Balasubramanian M, Fratzl-Zelman N, O'Sullivan R, Bull M, Fa Peel N, Pollitt RC, Jones R, Milne E, Smith K, Roschger P, Klaushofer K, Bishop NJ. Balasubramanian M, et al. Among authors: bull m. Am J Med Genet A. 2018 Jul;176(7):1578-1586. doi: 10.1002/ajmg.a.38830. Epub 2018 May 7. Am J Med Genet A. 2018. PMID: 29736964 Free article.
Expanding the phenotype of SPARC-related osteogenesis imperfecta: clinical findings in two patients with pathogenic variants in SPARC and literature review.
Durkin A, DeVile C, Arundel P, Bull M, Walsh J, Bishop NJ, Hupin E, Parekh S, Nadarajah R, Offiah AC, Calder A, Brock J, Baker D, Balasubramanian M. Durkin A, et al. Among authors: bull m. J Med Genet. 2022 Aug;59(8):810-816. doi: 10.1136/jmedgenet-2021-107942. Epub 2021 Aug 30. J Med Genet. 2022. PMID: 34462290 Free article. Review.
Translocation 1;7 in four cases of myeloid disorders.
Sheppard DM, Richkind KE, Bull M. Sheppard DM, et al. Among authors: bull m. Cancer Genet Cytogenet. 1989 Mar;38(1):49-52. doi: 10.1016/0165-4608(89)90164-7. Cancer Genet Cytogenet. 1989. PMID: 2713814
Spondylometepiphyseal dysplasia, Strudwick type.
Anderson CE, Sillence DO, Lachman RS, Toomey K, Bull M, Dorst J, Rimoin DL. Anderson CE, et al. Among authors: bull m. Am J Med Genet. 1982 Nov;13(3):243-56. doi: 10.1002/ajmg.1320130304. Am J Med Genet. 1982. PMID: 6817637
Peters anomaly with pulmonary hypoplasia.
Bull MJ, Baum JL. Bull MJ, et al. Birth Defects Orig Artic Ser. 1976;12(5):181-6. Birth Defects Orig Artic Ser. 1976. PMID: 953221 No abstract available.
503 results