Pagon RA - Search Results

1

Molecular detection of a translocation (Y;15) in a 45,X male.

Disteche CM, Brown L, Saal H, Friedman C, Thuline HC, Hoar DI, Pagon RA, Page DC. Disteche CM, et al. Among authors: pagon ra. Hum Genet. 1986 Dec;74(4):372-7. doi: 10.1007/BF00280488. Hum Genet. 1986. PMID: 3793100

2

Molecular analysis of 46,XY females and regional assignment of a new Y-chromosome-specific probe.

Cantrell MA, Bicknell JN, Pagon RA, Page DC, Walker DC, Saal HM, Zinn AB, Disteche CM. Cantrell MA, et al. Among authors: pagon ra. Hum Genet. 1989 Aug;83(1):88-92. doi: 10.1007/BF00274156. Hum Genet. 1989. PMID: 2570023

3

X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypes.

Disteche CM, Swisshelm K, Forbes S, Pagon RA. Disteche CM, et al. Among authors: pagon ra. Hum Genet. 1984;66(1):71-6. doi: 10.1007/BF00275190. Hum Genet. 1984. PMID: 6698557

4

Mapping of the distal boundary of the X-inactivation center in a rearranged X chromosome from a female expressing XIST.

Leppig KA, Brown CJ, Bressler SL, Gustashaw K, Pagon RA, Willard HF, Disteche CM. Leppig KA, et al. Among authors: pagon ra. Hum Mol Genet. 1993 Jul;2(7):883-7. doi: 10.1093/hmg/2.7.883. Hum Mol Genet. 1993. PMID: 8364571

5

Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.

Francke U, Ochs HD, de Martinville B, Giacalone J, Lindgren V, Distèche C, Pagon RA, Hofker MH, van Ommen GJ, Pearson PL, et al. Francke U, et al. Among authors: pagon ra. Am J Hum Genet. 1985 Mar;37(2):250-67. Am J Hum Genet. 1985. PMID: 4039107 Free PMC article.

6

Separation of retinoblastoma and esterase D loci in a patient with sporadic retinoblastoma and del(13)(q14.1q22.3).

Sparkes RS, Sparkes MC, Kalina RE, Pagon RA, Salk DJ, Disteche CM. Sparkes RS, et al. Among authors: pagon ra. Hum Genet. 1984;68(3):258-9. doi: 10.1007/BF00418397. Hum Genet. 1984. PMID: 6500578

7

Partial deletion of the long arm of chromosome 11 [del(11)(q23.3----qter)] with abnormal white matter.

Wardinsky TD, Weinberger E, Pagon RA, Clarren SK, Thuline HC. Wardinsky TD, et al. Among authors: pagon ra. Am J Med Genet. 1990 Jan;35(1):60-3. doi: 10.1002/ajmg.1320350111. Am J Med Genet. 1990. PMID: 2301470

8

Deletion mapping of H-Y antigen to the long arm of the human Y chromosome.

Cantrell MA, Bogan JS, Simpson E, Bicknell JN, Goulmy E, Chandler P, Pagon RA, Walker DC, Thuline HC, Graham JM Jr, et al. Cantrell MA, et al. Among authors: pagon ra. Genomics. 1992 Aug;13(4):1255-60. doi: 10.1016/0888-7543(92)90043-r. Genomics. 1992. PMID: 1505957 Free article.

9

Reevaluation of Russell-Silver syndrome.

Saal HM, Pagon RA, Pepin MG. Saal HM, et al. Among authors: pagon ra. J Pediatr. 1985 Nov;107(5):733-7. doi: 10.1016/s0022-3476(85)80402-9. J Pediatr. 1985. PMID: 2414426

10

Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1.

Scherer SW, Poorkaj P, Allen T, Kim J, Geshuri D, Nunes M, Soder S, Stephens K, Pagon RA, Patton MA, et al. Scherer SW, et al. Among authors: pagon ra. Am J Hum Genet. 1994 Jul;55(1):12-20. Am J Hum Genet. 1994. PMID: 8023840 Free PMC article. Review.

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