Gross A - Search Results

1

A genetic map of the mouse with 4,006 simple sequence length polymorphisms.

Dietrich WF, Miller JC, Steen RG, Merchant M, Damron D, Nahf R, Gross A, Joyce DC, Wessel M, Dredge RD, et al. Dietrich WF, et al. Among authors: gross a. Nat Genet. 1994 Jun;7(2 Spec No):220-45. doi: 10.1038/ng0694supp-220. Nat Genet. 1994. PMID: 7920646

2

Genetic linkage heterogeneity in the fragile X syndrome.

Brown WT, Gross AC, Chan CB, Jenkins EC. Brown WT, et al. Among authors: gross ac. Hum Genet. 1985;71(1):11-8. doi: 10.1007/BF00295659. Hum Genet. 1985. PMID: 2993154

3

Linkage in fragile X families of three distal flanking markers: ST14, DX13, and F8.

Brown WT, Gross AC, Goonewardena P, Ferrando C, Dobkin C, Jenkins EC. Brown WT, et al. Among authors: gross ac. Am J Med Genet. 1991 Feb-Mar;38(2-3):343-6. doi: 10.1002/ajmg.1320380235. Am J Med Genet. 1991. PMID: 1673308

4

Further evidence for genetic heterogeneity in the fragile X syndrome.

Brown WT, Jenkins EC, Gross AC, Chan CB, Krawczun MS, Duncan CJ, Sklower SL, Fisch GS. Brown WT, et al. Among authors: gross ac. Hum Genet. 1987 Apr;75(4):311-21. doi: 10.1007/BF00284100. Hum Genet. 1987. PMID: 2883105

5

DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity.

Brown WT, Gross AC, Chan CB, Jenkins EC. Brown WT, et al. Among authors: gross ac. Am J Med Genet. 1986 Jan-Feb;23(1-2):643-64. doi: 10.1002/ajmg.1320230158. Am J Med Genet. 1986. PMID: 3006490

6

Multilocus analysis of the fragile X syndrome.

Brown WT, Gross A, Chan C, Jenkins EC, Mandel JL, Oberlé I, Arveiler B, Novelli G, Thibodeau S, Hagerman R, et al. Brown WT, et al. Among authors: gross a. Hum Genet. 1988 Mar;78(3):201-5. doi: 10.1007/BF00291662. Hum Genet. 1988. PMID: 3162224

7

Multipoint linkage of 9 anonymous probes to HPRT, factor 9, and fragile X.

Brown WT, Ye W, Gross AC, Chan CB, Dobkin CS, Jenkins EC. Brown WT, et al. Among authors: gross ac. Am J Med Genet. 1988 May-Jun;30(1-2):551-66. doi: 10.1002/ajmg.1320300157. Am J Med Genet. 1988. PMID: 2902796

8

Detection of fragile X non-penetrant males by DNA marker analysis.

Brown WT, Gross A, Goonewardena P, Ferrando C, Dobkin C, Jenkins EC. Brown WT, et al. Among authors: gross a. Am J Med Genet. 1991 Feb-Mar;38(2-3):292-7. doi: 10.1002/ajmg.1320380226. Am J Med Genet. 1991. PMID: 1673300

9

RFLP analysis in 5 Sicilian families with the fragile X syndrome.

Romano V, Mascali G, Chiavetta V, Ragusa RM, Barletta C, Romano C, Mollica F, Mattina T, Gross A, Brown WT, et al. Romano V, et al. Among authors: gross a. Am J Med Genet. 1991 Feb-Mar;38(2-3):347-8. doi: 10.1002/ajmg.1320380236. Am J Med Genet. 1991. PMID: 1673309 No abstract available.

10

Linkage analysis of the fragile X syndrome using a new DNA marker U6.2 defining locus DXS304.

Goonewardena P, Brown WT, Gross AC, Ferrando C, Dobkin C, Romano V, Bosco P, Ceratto N, Pettersson U, Dahl N. Goonewardena P, et al. Among authors: gross ac. Am J Med Genet. 1991 Feb-Mar;38(2-3):322-7. doi: 10.1002/ajmg.1320380231. Am J Med Genet. 1991. PMID: 1673305

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