Ward K - Search Results

1

Diagnosis of neurofibromatosis I by using tightly linked, flanking DNA markers.

Ward K, O'Connell P, Carey JC, Leppert M, Jolley S, Plaetke R, Ogden B, White R. Ward K, et al. Am J Hum Genet. 1990 May;46(5):943-9. Am J Hum Genet. 1990. PMID: 1971145 Free PMC article.

2

A CA-repeat polymorphism close to the adenomatous polyposis coli (APC) gene offers improved diagnostic testing for familial APC.

Spirio L, Nelson L, Ward K, Burt R, White R, Leppert M. Spirio L, et al. Among authors: ward k. Am J Hum Genet. 1993 Feb;52(2):286-96. Am J Hum Genet. 1993. PMID: 8094265 Free PMC article.

3

Linkage disequilibrium in the neurofibromatosis 1 (NF1) region: implications for gene mapping.

Jorde LB, Watkins WS, Viskochil D, O'Connell P, Ward K. Jorde LB, et al. Among authors: ward k. Am J Hum Genet. 1993 Nov;53(5):1038-50. Am J Hum Genet. 1993. PMID: 8105688 Free PMC article.

4

Analysis of a Scottish founder effect narrows the TAPVR-1 gene interval to chromosome 4q12.

Bleyl SB, Botto LD, Carey JC, Young LT, Bamshad MJ, Leppert MF, Ward K. Bleyl SB, et al. Among authors: ward k. Am J Med Genet A. 2006 Nov 1;140(21):2368-73. doi: 10.1002/ajmg.a.31471. Am J Med Genet A. 2006. PMID: 17036341 No abstract available.

5

Xq28-linked noncompaction of the left ventricular myocardium: prenatal diagnosis and pathologic analysis of affected individuals.

Bleyl SB, Mumford BR, Brown-Harrison MC, Pagotto LT, Carey JC, Pysher TJ, Ward K, Chin TK. Bleyl SB, et al. Among authors: ward k. Am J Med Genet. 1997 Oct 31;72(3):257-65. Am J Med Genet. 1997. PMID: 9332651

6

Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome.

Bleyl SB, Mumford BR, Thompson V, Carey JC, Pysher TJ, Chin TK, Ward K. Bleyl SB, et al. Among authors: ward k. Am J Hum Genet. 1997 Oct;61(4):868-72. doi: 10.1086/514879. Am J Hum Genet. 1997. PMID: 9382097 Free PMC article.

7

Osteochondrodysplasia with rhizomelia, platyspondyly, callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension.

Faye-Petersen OM, Ward K, Carey JC, Knisely AS. Faye-Petersen OM, et al. Among authors: ward k. Am J Med Genet. 1991 Aug 1;40(2):183-7. doi: 10.1002/ajmg.1320400212. Am J Med Genet. 1991. PMID: 1897572

8

Familial total anomalous pulmonary venous return: a large Utah-Idaho family.

Bleyl S, Ruttenberg HD, Carey JC, Ward K. Bleyl S, et al. Among authors: ward k. Am J Med Genet. 1994 Oct 1;52(4):462-6. doi: 10.1002/ajmg.1320520412. Am J Med Genet. 1994. PMID: 7747759

9

A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12.

Bleyl S, Nelson L, Odelberg SJ, Ruttenberg HD, Otterud B, Leppert M, Ward K. Bleyl S, et al. Among authors: ward k. Am J Hum Genet. 1995 Feb;56(2):408-15. Am J Hum Genet. 1995. PMID: 7847375 Free PMC article.

10

Genetic heterogeneity in benign familial neonatal convulsions: identification of a new locus on chromosome 8q.

Lewis TB, Leach RJ, Ward K, O'Connell P, Ryan SG. Lewis TB, et al. Among authors: ward k. Am J Hum Genet. 1993 Sep;53(3):670-5. Am J Hum Genet. 1993. PMID: 8102508 Free PMC article.

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