Elliott AM - Search Results

1

Clinical and radiographic delineation of Bent Bone Dysplasia-FGFR2 type or Bent Bone Dysplasia with Distinctive Clavicles and Angel-shaped Phalanges.

Krakow D, Cohn DH, Wilcox WR, Noh GJ, Raffel LJ, Sarukhanov A, Ivanova MH, Danielpour M, Grange DK, Elliott AM, Bernstein JA, Rimoin DL, Merrill AE, Lachman RS. Krakow D, et al. Among authors: elliott am. Am J Med Genet A. 2016 Oct;170(10):2652-61. doi: 10.1002/ajmg.a.37772. Epub 2016 May 30. Am J Med Genet A. 2016. PMID: 27240702 Free PMC article.

2

Scapuloiliac dysostosis (Kosenow syndrome, pelvis-shoulder dysplasia) spectrum: three additional cases.

Elliott AM, Roeder ER, Witt DR, Rimoin DL, Lachman RS. Elliott AM, et al. Am J Med Genet. 2000 Dec 18;95(5):496-506. doi: 10.1002/1096-8628(20001218)95:5<496::aid-ajmg16>3.0.co;2-e. Am J Med Genet. 2000. PMID: 11146473

3

Cerebro-osseous-digital syndrome: four new cases of a lethal skeletal dysplasia--distinct from Neu-Laxova Syndrome.

Elliott AM, Gonzales M, Hoeffel JC, Le Merrer M, Maroteaux P, Encha-Razavi F, Joye N, Berchel C, Fliegel C, Aughton DJ, Beaudry-Rodgers K, Hasteh F, Nerlich AG, Wilcox WR, Rimoin DL, Lachman RS, Freisinger P. Elliott AM, et al. Am J Med Genet. 2002 Apr 22;109(2):139-48. doi: 10.1002/ajmg.10324. Am J Med Genet. 2002. PMID: 11977163

4

Spectrum of dolichospondylic dysplasia: two new patients with distinctive findings.

Elliott AM, Graham JM Jr, Curry CJ, Pal T, Rimoin DL, Lachman RS. Elliott AM, et al. Am J Med Genet. 2002 Dec 15;113(4):351-61. doi: 10.1002/ajmg.b.10656. Am J Med Genet. 2002. PMID: 12457407

5

Hand involvement in Schmid metaphyseal chondrodysplasia.

Elliott AM, Field FM, Rimoin DL, Lachman RS. Elliott AM, et al. Am J Med Genet A. 2005 Jan 15;132A(2):191-3. doi: 10.1002/ajmg.a.30433. Am J Med Genet A. 2005. PMID: 15578582

6

Osteocraniostenosis-hypomineralized skull with gracile long bones and splenic hypoplasia. Four new cases with distinctive chondro-osseous morphology.

Elliott AM, Wilcox WR, Spear GS, Field FM, Steffensen TS, Friedman BD, Rimoin DL, Lachman RS. Elliott AM, et al. Am J Med Genet A. 2006 Jul 15;140(14):1553-63. doi: 10.1002/ajmg.a.31326. Am J Med Genet A. 2006. PMID: 16770805

7

A distinctive type of metaphyseal chondrodysplasia with characteristic thickening of the distal ulna and radius: possible metaphyseal chondrodysplasia-Rosenberg.

Lee YS, Elliott AM, Loke KY, Lachman RS. Lee YS, et al. Among authors: elliott am. Am J Med Genet A. 2003 May 15;119A(1):50-6. doi: 10.1002/ajmg.a.20074. Am J Med Genet A. 2003. PMID: 12707959

8

Progressive erosive arthropathy with contractures, multicentric osteolysis-like changes, characteristic craniofacial appearance, and dermatological abnormalities: a new syndrome?

Teebi AS, Elliott AM, Azouz EM, Lachman RS. Teebi AS, et al. Among authors: elliott am. Am J Med Genet. 2001 May 1;100(3):198-203. doi: 10.1002/ajmg.1263. Am J Med Genet. 2001. PMID: 11343304

9

Derogatory nomenclature is still being used: the example of split hand/foot.

Elliott AM, Evans JA. Elliott AM, et al. Am J Med Genet A. 2015 Apr;167A(4):928-9. doi: 10.1002/ajmg.a.36952. Epub 2015 Mar 4. Am J Med Genet A. 2015. PMID: 25739702 No abstract available.

10

Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay.

Muller EA, Aradhya S, Atkin JF, Carmany EP, Elliott AM, Chudley AE, Clark RD, Everman DB, Garner S, Hall BD, Herman GE, Kivuva E, Ramanathan S, Stevenson DA, Stockton DW, Hudgins L. Muller EA, et al. Among authors: elliott am. Am J Med Genet A. 2012 Feb;158A(2):391-9. doi: 10.1002/ajmg.a.34216. Epub 2011 Dec 21. Am J Med Genet A. 2012. PMID: 22190277 Free article.

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