Adès LC - Search Results

1

Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28.

Adès LC, Gedeon AK, Wilson MJ, Latham M, Partington MW, Mulley JC, Nelson J, Lui K, Sillence DO. Adès LC, et al. Am J Med Genet. 1993 Feb 1;45(3):327-34. doi: 10.1002/ajmg.1320450309. Am J Med Genet. 1993. PMID: 8434619

2

Cardiofaciocutaneous syndrome.

Ades LC, Sillence DO, Rogers M. Ades LC, et al. Clin Dysmorphol. 1992 Jul;1(3):145-50. Clin Dysmorphol. 1992. PMID: 1342862

3

Agnathia-holoprosencephaly with tetramelia.

Ades LC, Sillence DO. Ades LC, et al. Clin Dysmorphol. 1992 Jul;1(3):182-4. Clin Dysmorphol. 1992. PMID: 1342869

4

Smith-Fineman-Myers syndrome in two brothers.

Adès LC, Kerr B, Turner G, Wise G. Adès LC, et al. Am J Med Genet. 1991 Sep 15;40(4):467-70. doi: 10.1002/ajmg.1320400419. Am J Med Genet. 1991. PMID: 1684092

5

Overlapping submicroscopic deletions in Xq28 in two unrelated boys with developmental disorders: identification of a gene near FRAXE.

Gedeon AK, Meinänen M, Adès LC, Kääriäinen H, Gécz J, Baker E, Sutherland GR, Mulley JC. Gedeon AK, et al. Among authors: ades lc. Am J Hum Genet. 1995 Apr;56(4):907-14. Am J Hum Genet. 1995. PMID: 7536393 Free PMC article.

6

Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndrome.

Adès LC, Morris LL, Power RG, Wilson M, Haan EA, Bateman JF, Milewicz DM, Sillence DO. Adès LC, et al. Am J Med Genet. 1995 Jul 17;57(4):565-72. doi: 10.1002/ajmg.1320570410. Am J Med Genet. 1995. PMID: 7573130 Review.

7

Localization of craniosynostosis Adelaide type to 4p16.

Hollway GE, Phillips HA, Adès LC, Haan EA, Mulley JC. Hollway GE, et al. Among authors: ades lc. Hum Mol Genet. 1995 Apr;4(4):681-3. doi: 10.1093/hmg/4.4.681. Hum Mol Genet. 1995. PMID: 7633418

8

Neurological involvement in Worth type endosteal hyperostosis: report of a family.

Adès LC, Morris LL, Burns R, Haan EA. Adès LC, et al. Am J Med Genet. 1994 May 15;51(1):46-50. doi: 10.1002/ajmg.1320510111. Am J Med Genet. 1994. PMID: 8030669

9

Jackson-Weiss syndrome: clinical and radiological findings in a large kindred and exclusion of the gene from 7p21 and 5qter.

Adès LC, Mulley JC, Senga IP, Morris LL, David DJ, Haan EA. Adès LC, et al. Am J Med Genet. 1994 Jun 1;51(2):121-30. doi: 10.1002/ajmg.1320510208. Am J Med Genet. 1994. PMID: 8092187

10

Polydactyly, campomelia, ambiguous genitalia, cystic dysplastic kidneys, and cerebral malformation in a fetus of consanguineous parents: a new multiple malformation syndrome, or a severe form of oral-facial-digital syndrome type IV?

Adès LC, Clapton WK, Morphett A, Morris LL, Haan EA. Adès LC, et al. Am J Med Genet. 1994 Jan 15;49(2):211-7. doi: 10.1002/ajmg.1320490211. Am J Med Genet. 1994. PMID: 8116671

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