Burn J - Search Results

1

Connexin43 mutations in sporadic and familial defects of laterality.

Splitt MP, Burn J, Goodship J. Splitt MP, et al. Among authors: burn j. N Engl J Med. 1995 Oct 5;333(14):941; author reply 941-2. N Engl J Med. 1995. PMID: 7666890 No abstract available.

2

Defects in the determination of left-right asymmetry.

Splitt MP, Burn J, Goodship J. Splitt MP, et al. Among authors: burn j. J Med Genet. 1996 Jun;33(6):498-503. doi: 10.1136/jmg.33.6.498. J Med Genet. 1996. PMID: 8782051 Free PMC article. Review. No abstract available.

3

Absence of mutations in the regulatory domain of the gap junction protein connexin 43 in patients with visceroatrial heterotaxy.

Penman Splitt M, Tsai MY, Burn J, Goodship JA. Penman Splitt M, et al. Among authors: burn j. Heart. 1997 Apr;77(4):369-70. doi: 10.1136/hrt.77.4.369. Heart. 1997. PMID: 9155619 Free PMC article.

4

UFD1L is not the monogenic basis for heart defects associated with the CATCH phenotype.

Goodship JA, Burn J. Goodship JA, et al. Among authors: burn j. Mol Med Today. 2000 Jan;6(1):14. doi: 10.1016/s1357-4310(99)01637-8. Mol Med Today. 2000. PMID: 10647129 No abstract available.

5

Deletions within chromosome 22q11 in familial congenital heart disease.

Wilson DI, Goodship JA, Burn J, Cross IE, Scambler PJ. Wilson DI, et al. Among authors: burn j. Lancet. 1992 Sep 5;340(8819):573-5. doi: 10.1016/0140-6736(92)92107-q. Lancet. 1992. PMID: 1355155

6

DiGeorge syndrome: part of CATCH 22.

Wilson DI, Burn J, Scambler P, Goodship J. Wilson DI, et al. Among authors: burn j. J Med Genet. 1993 Oct;30(10):852-6. doi: 10.1136/jmg.30.10.852. J Med Genet. 1993. PMID: 8230162 Free PMC article.

7

Developmental genetics of the heart.

Burn J, Goodship J. Burn J, et al. Curr Opin Genet Dev. 1996 Jun;6(3):322-5. doi: 10.1016/s0959-437x(96)80009-8. Curr Opin Genet Dev. 1996. PMID: 8791511 Review.

8

Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus.

Satoda M, Zhao F, Diaz GA, Burn J, Goodship J, Davidson HR, Pierpont ME, Gelb BD. Satoda M, et al. Among authors: burn j. Nat Genet. 2000 May;25(1):42-6. doi: 10.1038/75578. Nat Genet. 2000. PMID: 10802654

9

Genetic risks for children of women with myotonic dystrophy.

Goodship J, Gibson DE, Burn J, Honeyman J, Cubey RB, Schofield I. Goodship J, et al. Among authors: burn j. Am J Hum Genet. 1992 Jun;50(6):1340-2. Am J Hum Genet. 1992. PMID: 1530708 Free PMC article. No abstract available.

10

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.

Burn J, Takao A, Wilson D, Cross I, Momma K, Wadey R, Scambler P, Goodship J. Burn J, et al. J Med Genet. 1993 Oct;30(10):822-4. doi: 10.1136/jmg.30.10.822. J Med Genet. 1993. PMID: 8230157 Free PMC article.

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