Zackai EH - Search Results

1

The Philadelphia story: the 22q11.2 deletion: report on 250 patients.

McDonald-McGinn DM, Kirschner R, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Solot C, Wang P, Jacobs I, Handler S, Knightly C, Heher K, Wilson M, Ming JE, Grace K, Driscoll D, Pasquariello P, Randall P, Larossa D, Emanuel BS, Zackai EH. McDonald-McGinn DM, et al. Among authors: zackai eh. Genet Couns. 1999;10(1):11-24. Genet Couns. 1999. PMID: 10191425

2

Abnormal chromosome 22 and recurrence of trisomy-22 syndrome.

Emanuel BS, Zackai EH, Aronson MM, Mellman WJ, Moorhead PS. Emanuel BS, et al. Among authors: zackai eh. J Med Genet. 1976 Dec;13(6):501-6. doi: 10.1136/jmg.13.6.501. J Med Genet. 1976. PMID: 138742 Free PMC article.

3

Deletion mapping: further evidence for the location of acid phosphatase (ACP1) within 2p23.

Emanuel BS, Zackai EH, Van Dyke DC, Swallow DM, Allen FH, Mellman WJ. Emanuel BS, et al. Among authors: zackai eh. Am J Med Genet. 1979;4(2):167-72. doi: 10.1002/ajmg.1320040209. Am J Med Genet. 1979. PMID: 293131

4

Interstitial deletion 13q33 resulting from maternal insertional translocation.

Emanuel BS, Zackai EH, Moreau L, Coates P, Orrechio E. Emanuel BS, et al. Among authors: zackai eh. Clin Genet. 1979 Nov;16(5):340-6. doi: 10.1111/j.1399-0004.1979.tb01013.x. Clin Genet. 1979. PMID: 293234

5

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: zackai eh. Cytogenet Cell Genet. 1977;19(4):240. doi: 10.1159/000130815. Cytogenet Cell Genet. 1977. PMID: 598254 No abstract available.

6

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. Cytogenet Cell Genet. 1978;21(3):173. doi: 10.1159/000130891. Cytogenet Cell Genet. 1978. PMID: 657847 No abstract available.

7

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

8

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. Cytogenet Cell Genet. 1977;18(2):108. doi: 10.1159/000130755. Cytogenet Cell Genet. 1977. PMID: 862431 No abstract available.

9

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: zackai eh. Am J Med Genet. 1992 Sep 15;44(2):261-8. doi: 10.1002/ajmg.1320440237. Am J Med Genet. 1992. PMID: 1360769

10

Tricho-rhino-phalangeal syndrome type II (Langer-Giedion) with persistent cloaca and prune belly sequence in a girl with 8q interstitial deletion.

Ramos FJ, McDonald-McGinn DM, Emanuel BS, Zackai EH. Ramos FJ, et al. Among authors: zackai eh. Am J Med Genet. 1992 Dec 1;44(6):790-4. doi: 10.1002/ajmg.1320440614. Am J Med Genet. 1992. PMID: 1481848

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

653 results

Search Page