Hall C - Search Results

1

Elmslie FV, Vivian AJ, Gardiner H, Hall C, Mowat AP, Winter RM. Elmslie FV, et al. Among authors: hall c. J Med Genet. 1995 Apr;32(4):264-8. doi: 10.1136/jmg.32.4.264. J Med Genet. 1995. PMID: 7643353 Free PMC article.

2

New autosomal dominant form of spondyloepiphyseal dysplasia presenting with atlanto-axial instability.

Reardon W, Hall CM, Shaw DG, Kendall B, Hayward R, Winter RM. Reardon W, et al. Among authors: hall cm. Am J Med Genet. 1994 Oct 1;52(4):432-7. doi: 10.1002/ajmg.1320520408. Am J Med Genet. 1994. PMID: 7747755

3

Epiphyseal dysplasia of the femoral head, mild vertebral abnormality, myopia, and sensorineural deafness: report of a pedigree with autosomal dominant inheritance.

MacDermot KD, Roth SC, Hall C, Winter RM. MacDermot KD, et al. Among authors: hall c. J Med Genet. 1987 Oct;24(10):602-8. doi: 10.1136/jmg.24.10.602. J Med Genet. 1987. PMID: 3681905 Free PMC article.

4

The 3-M syndrome.

Winter RM, Baraitser M, Grant DB, Preece MA, Hall CM. Winter RM, et al. Among authors: hall cm. J Med Genet. 1984 Apr;21(2):124-8. doi: 10.1136/jmg.21.2.124. J Med Genet. 1984. PMID: 6716411 Free PMC article.

5

Mesomelic limb shortness: a previously unreported autosomal recessive type.

Reardon W, Hall CM, Slaney S, Huson SM, Connell J, al-Hilaly N, Fixsen J, Baraitser M, Winter RM. Reardon W, et al. Among authors: hall cm. Am J Med Genet. 1993 Oct 1;47(5):788-92. doi: 10.1002/ajmg.1320470537. Am J Med Genet. 1993. PMID: 8267013

6

Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis.

Reardon W, Wilkes D, Rutland P, Pulleyn LJ, Malcolm S, Dean JC, Evans RD, Jones BM, Hayward R, Hall CM, Nevin NC, Baraister M, Winter RM. Reardon W, et al. Among authors: hall cm. J Med Genet. 1997 Aug;34(8):632-6. doi: 10.1136/jmg.34.8.632. J Med Genet. 1997. PMID: 9279753 Free PMC article.

7

The Baller-Gerold syndrome: phenotypic and cytogenetic overlap with Roberts syndrome.

Huson SM, Rodgers CS, Hall CM, Winter RM. Huson SM, et al. Among authors: hall cm. J Med Genet. 1990 Jun;27(6):371-5. doi: 10.1136/jmg.27.6.371. J Med Genet. 1990. PMID: 2359099 Free PMC article.

8

The femoral hypoplasia-unusual facies syndrome.

Burn J, Winter RM, Baraitser M, Hall CM, Fixsen J. Burn J, et al. Among authors: hall cm. J Med Genet. 1984 Oct;21(5):331-40. doi: 10.1136/jmg.21.5.331. J Med Genet. 1984. PMID: 6502648 Free PMC article.

9

Extreme intrauterine growth retardation, hydrocephalus and aged facial appearance: a previously unrecognized autosomal recessive disorder?

Winter RM, Shortland D, Collins AL, Hall CM, Temple IK. Winter RM, et al. Among authors: hall cm. Clin Dysmorphol. 1996 Oct;5(4):313-9. Clin Dysmorphol. 1996. PMID: 8905196

10

Spectrum of craniosynostosis phenotypes associated with novel mutations at the fibroblast growth factor receptor 2 locus.

Pulleyn LJ, Reardon W, Wilkes D, Rutland P, Jones BM, Hayward R, Hall CM, Brueton L, Chun N, Lammer E, Malcolm S, Winter RM. Pulleyn LJ, et al. Among authors: hall cm. Eur J Hum Genet. 1996;4(5):283-91. doi: 10.1159/000472215. Eur J Hum Genet. 1996. PMID: 8946174

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