Mellman W - Search Results

1

A (10;17) translocation, balanced, 46 chromosomes. Repository identification No. GM-216.

Zackai E, Mellman W, Aronson M, Miller RC, Greene AE, Coriell LL. Zackai E, et al. Among authors: mellman w. Cytogenet Cell Genet. 1975;14(1):88-9. doi: 10.1159/000130326. Cytogenet Cell Genet. 1975. PMID: 1132254 No abstract available.

2

A (10;17) translocation, unbalanced, 46 chromosomes. Repository identification No. GM-217.

Zackai E, Mellman W, Aronson M, Miller RC, Greene AE, Coriell LL. Zackai E, et al. Among authors: mellman w. Cytogenet Cell Genet. 1975;14(1):90-1. doi: 10.1159/000130327. Cytogenet Cell Genet. 1975. PMID: 1132255 No abstract available.

3

A (13) terminal deletion, 46 chromosomes. Repository identification no. GM-250.

Aronson M, Zackai E, Mellman W, Miller RC, Greene AE, Coriell LL. Aronson M, et al. Among authors: mellman w. Cytogenet Cell Genet. 1975;15(1):57-8. doi: 10.1159/000130500. Cytogenet Cell Genet. 1975. PMID: 1183234 No abstract available.

4

A culture with a derivative chromosome 10 from a paternal (10;16) translocation. Repository identification no. GM-1396.

Emanuel B, Zackai EH, Mellman WJ, Aronson MM, Greene AE, Coriell LL. Emanuel B, et al. Among authors: mellman wj. Cytogenet Cell Genet. 1977;19(4):240. doi: 10.1159/000130815. Cytogenet Cell Genet. 1977. PMID: 598254 No abstract available.

5

A (14;20) translocation, unbalanced, from a subject with severe congenital anomalies. Respository identification No. GM-981.

Emanuel BS, Zackai E, Mellman WJ, Aronson MM, Greene AE, Coriell LL. Emanuel BS, et al. Among authors: mellman wj. Cytogenet Cell Genet. 1978;21(3):173. doi: 10.1159/000130891. Cytogenet Cell Genet. 1978. PMID: 657847 No abstract available.

6

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: mellman wj. Cytogenet Cell Genet. 1978;21(3):174. doi: 10.1159/000130892. Cytogenet Cell Genet. 1978. PMID: 657848 No abstract available.

7

Deletion of the short arm of chromosome 2 from a subject with congenital anomalies. Repository identification no. GM-1138.

Zackai E, Emanuel B, Mellman WJ, Aronson MM, Bozarth B, Greene AE, Coriell LL. Zackai E, et al. Among authors: mellman wj. Cytogenet Cell Genet. 1977;18(2):108. doi: 10.1159/000130755. Cytogenet Cell Genet. 1977. PMID: 862431 No abstract available.

8

A (10;17) translocation, 46 chromosomes. Repository identification No. GM-959.

Zackai EH, Moreno-Fuenmayer H, Mellman WJ, Aronson MM, Greene AE, Coriell LL. Zackai EH, et al. Among authors: mellman wj. Cytogenet Cell Genet. 1976;17(5):302-3. doi: 10.1159/000130729. Cytogenet Cell Genet. 1976. PMID: 1017324 No abstract available.

9

Galactosemia. Repository identification Nos. GM-52 and GM-53.

Mellman WJ, Tedesco TA, Greene AE, Coriell LL. Mellman WJ, et al. Cytogenet Cell Genet. 1975;15(3):198-9. doi: 10.1159/000130519. Cytogenet Cell Genet. 1975. PMID: 1192846 No abstract available.

10

Spontaneous D-G translocation in fibroblasts derived from a patient with trisomy 21 mosaicism.

Kohn G, Aronson M, Mellman WJ. Kohn G, et al. Among authors: mellman wj. Clin Genet. 1974;5(2):113-5. doi: 10.1111/j.1399-0004.1974.tb01671.x. Clin Genet. 1974. PMID: 4275246 No abstract available.

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