Seidman JG - Search Results

1

A nonsense mutation in MSX1 causes Witkop syndrome.

Jumlongras D, Bei M, Stimson JM, Wang WF, DePalma SR, Seidman CE, Felbor U, Maas R, Seidman JG, Olsen BR. Jumlongras D, et al. Among authors: seidman jg, seidman ce. Am J Hum Genet. 2001 Jul;69(1):67-74. doi: 10.1086/321271. Epub 2001 May 16. Am J Hum Genet. 2001. PMID: 11369996 Free PMC article.

2

A human MSX1 homeodomain missense mutation causes selective tooth agenesis.

Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE. Vastardis H, et al. Among authors: seidman jg, seidman ce. Nat Genet. 1996 Aug;13(4):417-21. doi: 10.1038/ng0896-417. Nat Genet. 1996. PMID: 8696335

3

Characterization of endoglin and identification of novel mutations in hereditary hemorrhagic telangiectasia.

Shovlin CL, Hughes JM, Scott J, Seidman CE, Seidman JG. Shovlin CL, et al. Among authors: seidman jg, seidman ce. Am J Hum Genet. 1997 Jul;61(1):68-79. doi: 10.1086/513906. Am J Hum Genet. 1997. PMID: 9245986 Free PMC article.

4

Pyogenic arthritis, pyoderma gangrenosum, and acne syndrome maps to chromosome 15q.

Yeon HB, Lindor NM, Seidman JG, Seidman CE. Yeon HB, et al. Among authors: seidman jg, seidman ce. Am J Hum Genet. 2000 Apr;66(4):1443-8. doi: 10.1086/302866. Epub 2000 Mar 21. Am J Hum Genet. 2000. PMID: 10729114 Free PMC article.

5

Assignment of a locus for dominantly inherited venous malformations to chromosome 9p.

Boon LM, Mulliken JB, Vikkula M, Watkins H, Seidman J, Olsen BR, Warman ML. Boon LM, et al. Hum Mol Genet. 1994 Sep;3(9):1583-7. doi: 10.1093/hmg/3.9.1583. Hum Mol Genet. 1994. PMID: 7833915

6

Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation.

Pollak MR, Brown EM, Estep HL, McLaine PN, Kifor O, Park J, Hebert SC, Seidman CE, Seidman JG. Pollak MR, et al. Among authors: seidman jg, seidman ce. Nat Genet. 1994 Nov;8(3):303-7. doi: 10.1038/ng1194-303. Nat Genet. 1994. PMID: 7874174

7

A dinucleotide repeat polymorphism in the MYBPH gene.

Watkins H, MacRae CA, Fischman DA, Seidman JG, Seidman CE. Watkins H, et al. Among authors: seidman jg, seidman ce. Hum Mol Genet. 1994 Dec;3(12):2267. doi: 10.1093/hmg/3.12.2267. Hum Mol Genet. 1994. PMID: 7881442 No abstract available.

8

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

Watkins H, MacRae C, Thierfelder L, Chou YH, Frenneaux M, McKenna W, Seidman JG, Seidman CE. Watkins H, et al. Among authors: seidman jg, seidman ce. Nat Genet. 1993 Apr;3(4):333-7. doi: 10.1038/ng0493-333. Nat Genet. 1993. PMID: 7981753

9

A dominant Stargardt's macular dystrophy locus maps to chromosome 13q34.

Zhang K, Bither PP, Park R, Donoso LA, Seidman JG, Seidman CE. Zhang K, et al. Among authors: seidman jg, seidman ce. Arch Ophthalmol. 1994 Jun;112(6):759-64. doi: 10.1001/archopht.1994.01090180057035. Arch Ophthalmol. 1994. PMID: 8002833

10

The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome).

Basson CT, Cowley GS, Solomon SD, Weissman B, Poznanski AK, Traill TA, Seidman JG, Seidman CE. Basson CT, et al. Among authors: seidman jg, seidman ce. N Engl J Med. 1994 Mar 31;330(13):885-91. doi: 10.1056/NEJM199403313301302. N Engl J Med. 1994. PMID: 8114858 Free article.

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