Spinner NB - Search Results

1

The role of cytologic NOR variants in the etiology of trisomy 21.

Spinner NB, Eunpu DL, Schmickel RD, Zackai EH, McEldrew D, Bunin GR, McDermid H, Emanuel BS. Spinner NB, et al. Am J Hum Genet. 1989 May;44(5):631-8. Am J Hum Genet. 1989. PMID: 2523191 Free PMC article. Review.

2

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome.

Driscoll DA, Spinner NB, Budarf ML, McDonald-McGinn DM, Zackai EH, Goldberg RB, Shprintzen RJ, Saal HM, Zonana J, Jones MC, et al. Driscoll DA, et al. Among authors: spinner nb. Am J Med Genet. 1992 Sep 15;44(2):261-8. doi: 10.1002/ajmg.1320440237. Am J Med Genet. 1992. PMID: 1360769

3

Frequency of the common fragile site at Xq27.2 under conditions of thymidylate stress: implications for cytogenetic diagnosis of the fragile-X syndrome.

Ramos FJ, Emanuel BS, Spinner NB. Ramos FJ, et al. Among authors: spinner nb. Am J Med Genet. 1992 Apr 1;42(6):835-8. doi: 10.1002/ajmg.1320420618. Am J Med Genet. 1992. PMID: 1532475

4

Holoprosencephaly in a newborn girl with 46,XX,i(18q).

Spinner NB, Eunpu DL, Austria JR, Mamunes P. Spinner NB, et al. Am J Med Genet. 1991 Apr 1;39(1):11-2. doi: 10.1002/ajmg.1320390104. Am J Med Genet. 1991. PMID: 1867253

5

A chromosomal breakage syndrome with profound immunodeficiency.

Conley ME, Spinner NB, Emanuel BS, Nowell PC, Nichols WW. Conley ME, et al. Among authors: spinner nb. Blood. 1986 May;67(5):1251-6. Blood. 1986. PMID: 2421804 Free article.

6

Cloning of a cDNA encoding the rat high molecular weight neurofilament peptide (NF-H): developmental and tissue expression in the rat, and mapping of its human homologue to chromosomes 1 and 22.

Lieberburg I, Spinner N, Snyder S, Anderson J, Goldgaber D, Smulowitz M, Carroll Z, Emanuel B, Breitner J, Rubin L. Lieberburg I, et al. Proc Natl Acad Sci U S A. 1989 Apr;86(7):2463-7. doi: 10.1073/pnas.86.7.2463. Proc Natl Acad Sci U S A. 1989. PMID: 2928342 Free PMC article.

7

Chronic myelomonocytic leukemia in a patient with a familial t(6;16)(q13;q22) translocation.

Spinner NB, Emanuel BS, Vonderheid EC, Nowell PC. Spinner NB, et al. Cancer Genet Cytogenet. 1987 Nov;29(1):159-64. doi: 10.1016/0165-4608(87)90044-6. Cancer Genet Cytogenet. 1987. PMID: 3478126

8

Molecular analysis of 24 Alagille syndrome families identifies a single submicroscopic deletion and further localizes the Alagille region within 20p12.

Rand EB, Spinner NB, Piccoli DA, Whitington PF, Taub R. Rand EB, et al. Among authors: spinner nb. Am J Hum Genet. 1995 Nov;57(5):1068-73. Am J Hum Genet. 1995. PMID: 7485156 Free PMC article.

9

Mosaic loss of 15q11q13 in a patient with hypomelanosis of Ito: is there a role for the P gene?

Pellegrino JE, Schnur RE, Kline R, Zackai EH, Spinner NB. Pellegrino JE, et al. Among authors: spinner nb. Hum Genet. 1995 Oct;96(4):485-9. doi: 10.1007/BF00191813. Hum Genet. 1995. PMID: 7557977

10

Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13.

Spinner NB, Zackai E, Cheng SD, Knoll JH. Spinner NB, et al. Am J Med Genet. 1995 May 22;57(1):61-5. doi: 10.1002/ajmg.1320570114. Am J Med Genet. 1995. PMID: 7645601

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