Wolff DJ - Search Results

1

Duplication 14(q24.3q31) in a father and daughter: delineation of a possible imprinted region.

Robin NH, Harari-Shacham A, Schwartz S, Wolff DJ. Robin NH, et al. Among authors: wolff dj. Am J Med Genet. 1997 Aug 22;71(3):361-5. doi: 10.1002/(sici)1096-8628(19970822)71:3<361::aid-ajmg20>3.0.co;2-h. Am J Med Genet. 1997. PMID: 9268110

2

Spontaneous and clastogen induced chromosomal breakage in scleroderma.

Wolff DJ, Needleman BW, Wasserman SS, Schwartz S. Wolff DJ, et al. J Rheumatol. 1991 Jun;18(6):837-40. J Rheumatol. 1991. PMID: 1716681

3

Characterization of Robertsonian translocations by using fluorescence in situ hybridization.

Wolff DJ, Schwartz S. Wolff DJ, et al. Am J Hum Genet. 1992 Jan;50(1):174-81. Am J Hum Genet. 1992. PMID: 1729886 Free PMC article.

4

Prenatal ascertainment of an inherited dup(18p) associated with an apparently normal phenotype.

Wolff DJ, Raffel LJ, Ferré MM, Schwartz S. Wolff DJ, et al. Am J Med Genet. 1991 Dec 1;41(3):319-21. doi: 10.1002/ajmg.1320410311. Am J Med Genet. 1991. PMID: 1789286 Review.

5

Analysis of centromeric activity in Robertsonian translocations: implications for a functional acrocentric hierarchy.

Sullivan BA, Wolff DJ, Schwartz S. Sullivan BA, et al. Among authors: wolff dj. Chromosoma. 1994 Dec;103(7):459-67. doi: 10.1007/BF00337384. Chromosoma. 1994. PMID: 7720412

6

Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.

Wolff DJ, Brown CJ, Schwartz S, Duncan AM, Surti U, Willard HF. Wolff DJ, et al. Am J Hum Genet. 1994 Jul;55(1):87-95. Am J Hum Genet. 1994. PMID: 8023855 Free PMC article. Review.

7

The effect of Robertsonian translocation on recombination on chromosome 21.

Wolff DJ, Schwartz S. Wolff DJ, et al. Hum Mol Genet. 1993 Jun;2(6):693-9. doi: 10.1093/hmg/2.6.693. Hum Mol Genet. 1993. PMID: 8102568

8

Precise mapping of a de novo duplication 18(q21-->q22) utilizing cytogenetic, biochemical, and molecular techniques.

Wolff DJ, Schwartz MF, Cohen MM, Schwartz S. Wolff DJ, et al. Am J Med Genet. 1993 Jun 15;46(5):520-3. doi: 10.1002/ajmg.1320460512. Am J Med Genet. 1993. PMID: 8322813

9

Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.

Wolff DJ, Miller AP, Van Dyke DL, Schwartz S, Willard HF. Wolff DJ, et al. Am J Hum Genet. 1996 Jan;58(1):154-60. Am J Hum Genet. 1996. PMID: 8554051 Free PMC article.

10

Cytogenetic and molecular genetic characterization of trisomy 20 mosaicism in fetal blood and tissues.

Micale MA, Wolff DJ, Dickerman LH, Redline R, Conroy JM, Schwartz S. Micale MA, et al. Among authors: wolff dj. Prenat Diagn. 1996 Oct;16(10):893-7. doi: 10.1002/(SICI)1097-0223(199610)16:10<893::AID-PD962>3.0.CO;2-M. Prenat Diagn. 1996. PMID: 8938057

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