Kerr B - Search Results

1

Costello syndrome: two cases with embryonal rhabdomyosarcoma.

Kerr B, Eden OB, Dandamudi R, Shannon N, Quarrell O, Emmerson A, Ladusans E, Gerrard M, Donnai D. Kerr B, et al. J Med Genet. 1998 Dec;35(12):1036-9. doi: 10.1136/jmg.35.12.1036. J Med Genet. 1998. PMID: 9863604 Free PMC article.

2

Smith-Fineman-Myers syndrome in two brothers.

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

3

Rothmund-Thomson syndrome: two case reports show heterogeneous cutaneous abnormalities, an association with genetically programmed ageing changes, and increased chromosomal radiosensitivity.

Kerr B, Ashcroft GS, Scott D, Horan MA, Ferguson MW, Donnai D. Kerr B, et al. J Med Genet. 1996 Nov;33(11):928-34. doi: 10.1136/jmg.33.11.928. J Med Genet. 1996. PMID: 8950673 Free PMC article.

4

Macrocephaly with cutis marmorata, haemangioma and syndactyly--a distinctive overgrowth syndrome.

Clayton-Smith J, Kerr B, Brunner H, Tranebjaerg L, Magee A, Hennekam RC, Mueller RF, Brueton L, Super M, Steen-Johnsen J, Donnai D. Clayton-Smith J, et al. Among authors: kerr b. Clin Dysmorphol. 1997 Oct;6(4):291-302. doi: 10.1097/00019605-199710000-00001. Clin Dysmorphol. 1997. PMID: 9354837

5

Choanal atresia and hypothelia following methimazole exposure in utero: a second report.

Wilson LC, Kerr BA, Wilkinson R, Fossard C, Donnai D. Wilson LC, et al. Among authors: kerr ba. Am J Med Genet. 1998 Jan 13;75(2):220-2. doi: 10.1002/(sici)1096-8628(19980113)75:2<220::aid-ajmg21>3.0.co;2-q. Am J Med Genet. 1998. PMID: 9450891

6

Spondylometaphyseal dysplasia Sedaghatian type associated with lethal arrhythmia and normal intrauterine growth in three siblings.

Kerr B, Smith V, Patel R, Ladusans E, Sillence DO. Kerr B, et al. Clin Dysmorphol. 2000 Jul;9(3):167-72. doi: 10.1097/00019605-200009030-00003. Clin Dysmorphol. 2000. PMID: 10955475

7

Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein.

Watson P, Black G, Ramsden S, Barrow M, Super M, Kerr B, Clayton-Smith J. Watson P, et al. Among authors: kerr b. J Med Genet. 2001 Apr;38(4):224-8. doi: 10.1136/jmg.38.4.224. J Med Genet. 2001. PMID: 11283202 Free PMC article.

8

Domain disruption and mutation of the bZIP transcription factor, MAF, associated with cataract, ocular anterior segment dysgenesis and coloboma.

Jamieson RV, Perveen R, Kerr B, Carette M, Yardley J, Heon E, Wirth MG, van Heyningen V, Donnai D, Munier F, Black GC. Jamieson RV, et al. Among authors: kerr b. Hum Mol Genet. 2002 Jan 1;11(1):33-42. doi: 10.1093/hmg/11.1.33. Hum Mol Genet. 2002. PMID: 11772997

9

Chromosomal translocation in a family with ocular anomalies: indications for karyotype analysis.

Jamieson RV, Gaunt L, Donnai D, Black GC, Kerr B, Stecko O, Black GC. Jamieson RV, et al. Among authors: kerr b. Br J Ophthalmol. 2003 May;87(5):646-8. doi: 10.1136/bjo.87.5.646-a. Br J Ophthalmol. 2003. PMID: 12714415 Free PMC article. No abstract available.

10

Further delineation of the phenotype associated with heterozygous mutations in ZFHX1B.

Wilson M, Mowat D, Dastot-Le Moal F, Cacheux V, Kääriäinen H, Cass D, Donnai D, Clayton-Smith J, Townshend S, Curry C, Gattas M, Braddock S, Kerr B, Aftimos S, Zehnwirth H, Barrey C, Goossens M. Wilson M, et al. Among authors: kerr b. Am J Med Genet A. 2003 Jun 15;119A(3):257-65. doi: 10.1002/ajmg.a.20053. Am J Med Genet A. 2003. PMID: 12784289

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