Strain L - Search Results

1

Fragile X syndrome with FMR1 and FMR2 deletion.

Moore SJ, Strain L, Cole GF, Miedzybrodzka Z, Kelly KF, Dean JC. Moore SJ, et al. Among authors: strain l. J Med Genet. 1999 Jul;36(7):565-6. J Med Genet. 1999. PMID: 10424820 Free PMC article.

2

A true hermaphrodite chimera resulting from embryo amalgamation after in vitro fertilization.

Strain L, Dean JC, Hamilton MP, Bonthron DT. Strain L, et al. N Engl J Med. 1998 Jan 15;338(3):166-9. doi: 10.1056/NEJM199801153380305. N Engl J Med. 1998. PMID: 9428825 Free article. No abstract available.

3

Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22.

Strain L, Wright AF, Bonthron DT. Strain L, et al. J Med Genet. 1997 Jul;34(7):535-40. doi: 10.1136/jmg.34.7.535. J Med Genet. 1997. PMID: 9222959 Free PMC article.

4

Keratosis follicularis spinulosa decalvans: confirmation of linkage to Xp22.13-p22.2.

Porteous ME, Strain L, Logie LJ, Herd RM, Benton EC. Porteous ME, et al. Among authors: strain l. J Med Genet. 1998 Apr;35(4):336-7. doi: 10.1136/jmg.35.4.336. J Med Genet. 1998. PMID: 9598732 Free PMC article.

5

Factors determining penetrance in familial atypical haemolytic uraemic syndrome.

Sansbury FH, Cordell HJ, Bingham C, Bromilow G, Nicholls A, Powell R, Shields B, Smyth L, Warwicker P, Strain L, Wilson V, Goodship JA, Goodship TH, Turnpenny PD. Sansbury FH, et al. Among authors: strain l. J Med Genet. 2014 Nov;51(11):756-64. doi: 10.1136/jmedgenet-2014-102498. Epub 2014 Sep 26. J Med Genet. 2014. PMID: 25261570

6

Discordant segregation of Xq28 markers and a mutation in the L1 gene in a family with X linked hydrocephalus.

Jouet M, Strain L, Bonthron D, Kenwrick S. Jouet M, et al. Among authors: strain l. J Med Genet. 1996 Mar;33(3):248-50. doi: 10.1136/jmg.33.3.248. J Med Genet. 1996. PMID: 8728703 Free PMC article.

7

Neurogenic chronic idiopathic intestinal pseudo-obstruction, patent ductus arteriosus, and thrombocytopenia segregating as an X linked recessive disorder.

FitzPatrick DR, Strain L, Thomas AE, Barr DG, Todd A, Smith NM, Scobie WG. FitzPatrick DR, et al. Among authors: strain l. J Med Genet. 1997 Aug;34(8):666-9. doi: 10.1136/jmg.34.8.666. J Med Genet. 1997. PMID: 9279759 Free PMC article.

8

A novel atypical 22q11.2 distal deletion in father and son.

Garcia-Miñaur S, Fantes J, Murray RS, Porteous ME, Strain L, Burns JE, Stephen J, Warner JP. Garcia-Miñaur S, et al. Among authors: strain l. J Med Genet. 2002 Oct;39(10):E62. doi: 10.1136/jmg.39.10.e62. J Med Genet. 2002. PMID: 12362044 Free PMC article. No abstract available.

9

Confirmation of prenatal diagnosis of cystic fibrosis by DNA typing of fetal tissues.

Curtis A, Strain L, Mennie M, Brock DJ. Curtis A, et al. Among authors: strain l. J Med Genet. 1988 Feb;25(2):79-82. doi: 10.1136/jmg.25.2.79. J Med Genet. 1988. PMID: 2894468 Free PMC article.

10

Prenatal diagnosis of fragile X syndrome: management of the male fetus with a premutation.

Strain L, Porteous ME, Gosden CM, Ellis PM, Neilson JP, Bonthron DT. Strain L, et al. Prenat Diagn. 1994 Jun;14(6):469-74. doi: 10.1002/pd.1970140610. Prenat Diagn. 1994. PMID: 7937584

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