Rimoin DL - Search Results

1

Spondylometaphyseal dysplasia, Sedaghatian type.

Peeden JN Jr, Rimoin DL, Lachman RS, Dyer ML, Gerard D, Gruber HE. Peeden JN Jr, et al. Among authors: rimoin dl. Am J Med Genet. 1992 Nov 15;44(5):651-6. doi: 10.1002/ajmg.1320440525. Am J Med Genet. 1992. PMID: 1481828

2

Possible heterogeneity in spondyloenchondrodysplasia: quadriparesis, basal ganglia calcifications, and chondrocyte inclusions.

Frydman M, Bar-Ziv J, Preminger-Shapiro R, Brezner A, Brand N, Ben-Ami T, Lachman RS, Gruber HE, Rimoin DL. Frydman M, et al. Among authors: rimoin dl. Am J Med Genet. 1990 Jul;36(3):279-84. doi: 10.1002/ajmg.1320360306. Am J Med Genet. 1990. PMID: 2363422

3

Brachyolmia: radiographic and genetic evidence of heterogeneity.

Shohat M, Lachman R, Gruber HE, Rimoin DL. Shohat M, et al. Among authors: rimoin dl. Am J Med Genet. 1989 Jun;33(2):209-19. doi: 10.1002/ajmg.1320330214. Am J Med Genet. 1989. PMID: 2669482 Review.

4

Microcephalic osteodysplastic dysplasia.

Hersh JH, Joyce MR, Spranger J, Goatley EC, Lachman RS, Bhatt S, Rimoin DL. Hersh JH, et al. Among authors: rimoin dl. Am J Med Genet. 1994 Jul 1;51(3):194-9. doi: 10.1002/ajmg.1320510304. Am J Med Genet. 1994. PMID: 8074143

5

Hydrops-ectopic calcification-moth-eaten skeletal dysplasia (Greenberg dysplasia): prenatal diagnosis and further delineation of a rare genetic disorder.

Chitayat D, Gruber H, Mullen BJ, Pauzner D, Costa T, Lachman R, Rimoin DL. Chitayat D, et al. Among authors: rimoin dl. Am J Med Genet. 1993 Aug 15;47(2):272-7. doi: 10.1002/ajmg.1320470226. Am J Med Genet. 1993. PMID: 8213919 Review.

6

New epiphyseal stippling syndrome with osteoclastic hyperplasia.

Shohat M, Rimoin DL, Gruber HE, Lachman R. Shohat M, et al. Among authors: rimoin dl. Am J Med Genet. 1993 Mar 1;45(5):558-61. doi: 10.1002/ajmg.1320450506. Am J Med Genet. 1993. PMID: 8456823

7

Gracile bone dysplasia.

Thomas JA, Rimoin DL, Lachman RS, Wilcox WR. Thomas JA, et al. Among authors: rimoin dl. Am J Med Genet. 1998 Jan 6;75(1):95-100. Am J Med Genet. 1998. PMID: 9450865

8

Pacman dysplasia: report of two affected sibs.

Wilcox WR, Lucas BC, Loebel B, Bachman RP, Lachman RS, Rimoin DL. Wilcox WR, et al. Among authors: rimoin dl. Am J Med Genet. 1998 May 26;77(4):272-6. Am J Med Genet. 1998. PMID: 9600734

9

Radiographic and morphologic findings in a previously undescribed type of mesomelic dysplasia resembling atelosteogenesis type II.

Brodie SG, Lachman RS, Crandall BF, Fox MA, Rimoin DL, Cohn DH, Wilcox WR. Brodie SG, et al. Among authors: rimoin dl. Am J Med Genet. 1998 Nov 16;80(3):247-51. Am J Med Genet. 1998. PMID: 9843047

10

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. Among authors: rimoin dl. Am J Med Genet. 2002 Dec 15;113(4):351-61. doi: 10.1002/ajmg.b.10656. Am J Med Genet. 2002. PMID: 12457407

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