Slaney S - Search Results

1

Baraitser M, Dossetor J, Slaney S, Green A. Baraitser M, et al. Among authors: slaney s. Acta Ophthalmol Scand Suppl. 1996;(219):8-10. doi: 10.1111/j.1600-0420.1996.tb00372.x. Acta Ophthalmol Scand Suppl. 1996. PMID: 8741105 No abstract available.

2

Severe microcephaly, choreiform movements, cataracts and sensorineural deafness in two patients: a new syndrome?

Plomp AS, Baraitser M, Slaney SF, Winter RM. Plomp AS, et al. Among authors: slaney sf. Clin Dysmorphol. 2000 Jan;9(1):11-4. doi: 10.1097/00019605-200009010-00002. Clin Dysmorphol. 2000. PMID: 10649790

3

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: slaney s. Am J Med Genet. 1993 Oct 1;47(5):788-92. doi: 10.1002/ajmg.1320470537. Am J Med Genet. 1993. PMID: 8267013

4

Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes.

Rutland P, Pulleyn LJ, Reardon W, Baraitser M, Hayward R, Jones B, Malcolm S, Winter RM, Oldridge M, Slaney SF, et al. Rutland P, et al. Among authors: slaney sf. Nat Genet. 1995 Feb;9(2):173-6. doi: 10.1038/ng0295-173. Nat Genet. 1995. PMID: 7719345

5

A new syndrome of short stature, distinctive facial features and periventricular grey matter heterotopia.

Slaney SF, Chong WK, Winter RM. Slaney SF, et al. Clin Dysmorphol. 1999 Jan;8(1):5-9. Clin Dysmorphol. 1999. PMID: 10327244

6

A new syndrome of spondyloepimetaphyseal dysplasia, eczema and hypogammaglobulinaemia.

Slaney SF, Hall CM, Atherton DJ, Winter RM. Slaney SF, et al. Clin Dysmorphol. 1999 Apr;8(2):79-85. Clin Dysmorphol. 1999. PMID: 10319195

7

Congenital cervical spinal fusion: a study in Apert syndrome.

Thompson DN, Slaney SF, Hall CM, Shaw D, Jones BM, Hayward RD. Thompson DN, et al. Among authors: slaney sf. Pediatr Neurosurg. 1996 Jul;25(1):20-7. doi: 10.1159/000121091. Pediatr Neurosurg. 1996. PMID: 9055330

8

Parent-child transmission of infantile cholestasis with lymphoedema (Aagenaes syndrome).

Morris AA, Sequeira JS, Malone M, Slaney SF, Clayton PT. Morris AA, et al. Among authors: slaney sf. J Med Genet. 1997 Oct;34(10):852-3. doi: 10.1136/jmg.34.10.852. J Med Genet. 1997. PMID: 9350821 Free PMC article.

9

Lethal micromelic short-rib skeletal dysplasia with triangular-shaped humerus.

Slaney SF, Sprigg A, Davies NP, Hall CM. Slaney SF, et al. Pediatr Radiol. 1999 Nov;29(11):835-7. doi: 10.1007/s002470050707. Pediatr Radiol. 1999. PMID: 10552063

10

Another case of the autosomal recessive Weaver-like syndrome.

Slaney SF, Winter RM. Slaney SF, et al. Am J Med Genet. 1997 Oct 31;72(3):369-70. Am J Med Genet. 1997. PMID: 9332672 No abstract available.

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