Whyte MP - Search Results

1

Gnathodiaphyseal dysplasia: Severe atypical presentation with novel heterozygous mutation of the anoctamin gene (ANO5).

Otaify GA, Whyte MP, Gottesman GS, McAlister WH, Eric Gordon J, Hollander A, Andrews MV, El-Mofty SK, Chen WS, Veis DV, Stolina M, Woo AS, Katsonis P, Lichtarge O, Zhang F, Shinawi M. Otaify GA, et al. Among authors: whyte mp. Bone. 2018 Feb;107:161-171. doi: 10.1016/j.bone.2017.11.012. Epub 2017 Nov 21. Bone. 2018. PMID: 29175271 Free PMC article.

2

Occipital horn syndrome. Additional radiographic findings in two new cases.

Herman TE, McAlister WH, Boniface A, Whyte MP. Herman TE, et al. Among authors: whyte mp. Pediatr Radiol. 1992;22(5):363-5. doi: 10.1007/BF02016258. Pediatr Radiol. 1992. PMID: 1408447

3

Hypotrichosis with spondyloepimetaphyseal dysplasia in three generations: a new autosomal dominant syndrome.

Whyte MP, Petersen DJ, McAlister WH. Whyte MP, et al. Am J Med Genet. 1990 Jul;36(3):288-91. doi: 10.1002/ajmg.1320360308. Am J Med Genet. 1990. PMID: 2363424

4

Central osteosclerosis with ectodermal dysplasia: clinical, laboratory, radiologic, and histopathologic characterization with review of the literature.

Civitelli R, McAlister WH, Teitelbaum SL, Whyte MP. Civitelli R, et al. Among authors: whyte mp. J Bone Miner Res. 1989 Dec;4(6):863-75. doi: 10.1002/jbmr.5650040611. J Bone Miner Res. 1989. PMID: 2692405 Review.

5

Tibial bowing exacerbated by partial premature epiphyseal closure in sex-linked hypophosphatemic rickets.

McAlister WH, Kim GS, Whyte MP. McAlister WH, et al. Among authors: whyte mp. Radiology. 1987 Feb;162(2):461-3. doi: 10.1148/radiology.162.2.3025921. Radiology. 1987. PMID: 3025921

6

Macroepiphyseal dysplasia with symptomatic osteoporosis, wrinkled skin, and aged appearance: a presumed autosomal recessive condition.

McAlister WH, Coe JD, Whyte MP. McAlister WH, et al. Among authors: whyte mp. Skeletal Radiol. 1986;15(1):47-51. doi: 10.1007/BF00355073. Skeletal Radiol. 1986. PMID: 3941923

7

Intermittent radiographic changes of rickets without defective trabecular bone mineralization in a case of spondylometaphyseal dysplasia.

Kim GS, McAlister WH, Whyte MP. Kim GS, et al. Among authors: whyte mp. Bone. 1986;7(1):1-7. doi: 10.1016/8756-3282(86)90144-4. Bone. 1986. PMID: 3964492

8

Hypercalciuria in osteogenesis imperfecta: a follow-up study to assess renal effects.

Chines A, Boniface A, McAlister W, Whyte M. Chines A, et al. Bone. 1995 Mar;16(3):333-9. doi: 10.1016/8756-3282(94)00046-8. Bone. 1995. PMID: 7786636

9

Spondyloepimetaphyseal dysplasia: clinical and radiologic investigation of a large kindred manifesting autosomal dominant inheritance, and a review of the literature.

Patel AC, McAlister WH, Whyte MP. Patel AC, et al. Among authors: whyte mp. Medicine (Baltimore). 1993 Sep;72(5):326-42. Medicine (Baltimore). 1993. PMID: 8412645 Review.

10

Juvenile Paget disease: life-long features of a mildly affected young woman.

Golob DS, McAlister WH, Mills BG, Fedde KN, Reinus WR, Teitelbaum SL, Beeki S, Whyte MP. Golob DS, et al. Among authors: whyte mp. J Bone Miner Res. 1996 Jan;11(1):132-42. doi: 10.1002/jbmr.5650110118. J Bone Miner Res. 1996. PMID: 8770706

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