Seidman JG - Search Results

1

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.

2

A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3.

Shovlin CL, Hughes JM, Tuddenham EG, Temperley I, Perembelon YF, Scott J, Seidman CE, Seidman JG. Shovlin CL, et al. Among authors: seidman jg, seidman ce. Nat Genet. 1994 Feb;6(2):205-9. doi: 10.1038/ng0294-205. Nat Genet. 1994. PMID: 8162076

3

Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy.

Watkins H, Thierfelder L, Anan R, Jarcho J, Matsumori A, McKenna W, Seidman JG, Seidman CE. Watkins H, et al. Among authors: seidman jg, seidman ce. Am J Hum Genet. 1993 Dec;53(6):1180-5. Am J Hum Genet. 1993. PMID: 8250038 Free PMC article.

4

Hereditary inclusion body myopathy maps to chromosome 9p1-q1.

Mitrani-Rosenbaum S, Argov Z, Blumenfeld A, Seidman CE, Seidman JG. Mitrani-Rosenbaum S, et al. Among authors: seidman jg, seidman ce. Hum Mol Genet. 1996 Jan;5(1):159-163. doi: 10.1093/hmg/5.1.159. Hum Mol Genet. 1996. PMID: 8789455

5

The Bjornstad syndrome (sensorineural hearing loss and pili torti) disease gene maps to chromosome 2q34-36.

Lubianca Neto JF, Lu L, Eavey RD, Flores MA, Caldera RM, Sangwatanaroj S, Schott JJ, McDonough B, Santos JI, Seidman CE, Seidman JG. Lubianca Neto JF, et al. Among authors: seidman jg, seidman ce. Am J Hum Genet. 1998 May;62(5):1107-12. doi: 10.1086/301837. Am J Hum Genet. 1998. PMID: 9545407 Free PMC article.

6

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.

7

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.

8

Phenotypic diversity in hypertrophic cardiomyopathy.

Arad M, Seidman JG, Seidman CE. Arad M, et al. Among authors: seidman jg, seidman ce. Hum Mol Genet. 2002 Oct 1;11(20):2499-506. doi: 10.1093/hmg/11.20.2499. Hum Mol Genet. 2002. PMID: 12351586 Review.

9

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

10

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.

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