Coriell LL - Search Results

1

A (14;20) balanced translocation, 46, XX. Repository identification No. GM-982.

Emanuel BS, Zackai E, Mellman WJ, Aronson MM, Greene AE, Coriell LL. Emanuel BS, et al. Among authors: coriell ll. Cytogenet Cell Genet. 1978;21(3):174. doi: 10.1159/000130892. Cytogenet Cell Genet. 1978. PMID: 657848 No abstract available.

2

An (8;12) translocation, balanced, 46 chromosomes. Repository identification No. GM-213.

Lin CC, Uchida I, Hotz H, Miller RC, Greene AE, Coriell LL. Lin CC, et al. Among authors: coriell ll. Cytogenet Cell Genet. 1975;14(1):78-9. doi: 10.1159/000130321. Cytogenet Cell Genet. 1975. PMID: 124242 No abstract available.

3

Interstitial deletion in the long arm of chromosome 1 in a subject with congenital abnormalities. Repository identification No. GM-214.

de la Chapelle A, Koivisto M, Aronson MM, Greene AE, Coriell LL. de la Chapelle A, et al. Among authors: coriell ll. Cytogenet Cell Genet. 1979;23(3):220. doi: 10.1159/000131330. Cytogenet Cell Genet. 1979. PMID: 436455 No abstract available.

4

Recombinant chromosome 13 with a duplication of a short arm. Repository identification No. GM-1570.

Seabright M, Gregson N, Aronson MM, Greene AE, Coriell LL. Seabright M, et al. Among authors: coriell ll. Cytogenet Cell Genet. 1979;23(4):281. doi: 10.1159/000131341. Cytogenet Cell Genet. 1979. PMID: 446098 No abstract available.

5

A (4;10) translocation, balanced, 46 chromosomes. Repository identification No. GM-1091.

Hsu LY, Hirschhorn K, Aronson MM, Greene AE, Coriell LL. Hsu LY, et al. Among authors: coriell ll. Cytogenet Cell Genet. 1979;23(4):282. doi: 10.1159/000131342. Cytogenet Cell Genet. 1979. PMID: 446099 No abstract available.

6

A (1;6) balanced translocation, 46 chromosomes. Repository identification No. GM-1421.

Rary J, Hill R, Aronson MM, Greene AE, Coriell LL. Rary J, et al. Among authors: coriell ll. Cytogenet Cell Genet. 1979;23(4):283. doi: 10.1159/000131343. Cytogenet Cell Genet. 1979. PMID: 446100 No abstract available.

7

A 13;13 tandem chromosome translocation in a subject with congenital anomalies. Repository identification No. GM-2018.

Kohn G, Cohen MM, Aronson MM, Greene AE, Coriell LL. Kohn G, et al. Among authors: coriell ll. Cytogenet Cell Genet. 1979;24(1):72. doi: 10.1159/000131359. Cytogenet Cell Genet. 1979. PMID: 456042 No abstract available.

8

A (7;18) translocation. 46,XY. Repository identification No. GM-657.

Punnett HH, Kistenmacher ML, Miller RC, Greene AE, Coriell LL. Punnett HH, et al. Among authors: coriell ll. Cytogenet Cell Genet. 1979;24(2):126. doi: 10.1159/000131366. Cytogenet Cell Genet. 1979. PMID: 477406 No abstract available.

9

Duplication of a segment of chromosome 3 in a subject with multiple congenital anomalies and a 47,XYY father, inversion of chromosomes 3 and 9 in the mother, and inversion of chromosome 9 in a brother. Repository identification Nos. GM-1253, GM-1252, and GM-1251.

Pope IS, Thuline HC, Aronson MM, Bozarth B, Greene AE, Coriell LL. Pope IS, et al. Among authors: coriell ll. Cytogenet Cell Genet. 1979;24(2):127-8. doi: 10.1159/000131367. Cytogenet Cell Genet. 1979. PMID: 477407 No abstract available.

10

A derivative chromosome 13pat in a subject with multiple congenital abnormalities. Repository identification No. GM-1224.

Kohn G, Cohen MM, Aronson MM, Greene AE, Coriell LL. Kohn G, et al. Among authors: coriell ll. Cytogenet Cell Genet. 1979;24(3):197. doi: 10.1159/000131377. Cytogenet Cell Genet. 1979. PMID: 477416 No abstract available.

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