Zackowski JL - Search Results

1

Reproductive outcome in 3 families with a satellited chromosome 4 with review of the literature.

Arn PH, Younie L, Russo S, Zackowski JL, Mankinen C, Estabrooks L. Arn PH, et al. Among authors: zackowski jl. Am J Med Genet. 1995 Jul 3;57(3):420-4. doi: 10.1002/ajmg.1320570311. Am J Med Genet. 1995. PMID: 7677144 Review.

2

Preaxial acrofacial dysostosis (Nager syndrome) associated with an inherited and apparently balanced X;9 translocation: prenatal and postnatal late replication studies.

Zori RT, Gray BA, Bent-Williams A, Driscoll DJ, Williams CA, Zackowski JL. Zori RT, et al. Among authors: zackowski jl. Am J Med Genet. 1993 Jun 1;46(4):379-83. doi: 10.1002/ajmg.1320460407. Am J Med Genet. 1993. PMID: 8357008

3

Proximal interstitial deletion of 7q: a case report and review of the literature.

Zackowski JL, Raffel LJ, Blank CA, Schwartz S. Zackowski JL, et al. Am J Med Genet. 1990 Jul;36(3):328-32. doi: 10.1002/ajmg.1320360317. Am J Med Genet. 1990. PMID: 2194394 Review.

4

Sex chromosome markers: characterization using fluorescence in situ hybridization and review of the literature.

Schwartz S, Depinet TW, Leana-Cox J, Isada NB, Karson EM, Park VM, Pasztor LM, Sheppard LC, Stallard R, Wolff DJ, Zinn AB, Zurcher VL, Zackowski JL. Schwartz S, et al. Among authors: zackowski jl. Am J Med Genet. 1997 Jul 11;71(1):1-7. doi: 10.1002/(sici)1096-8628(19970711)71:1<1::aid-ajmg1>3.0.co;2-1. Am J Med Genet. 1997. PMID: 9215760 Review.

5

Random X inactivation in a girl with a balanced t(X;9) and an abnormal phenotype.

Wolff DJ, Schwartz S, Montgomery T, Zackowski JL. Wolff DJ, et al. Among authors: zackowski jl. Am J Med Genet. 1998 Jun 5;77(5):401-4. doi: 10.1002/(sici)1096-8628(19980605)77:5<401::aid-ajmg9>3.0.co;2-p. Am J Med Genet. 1998. PMID: 9632170

6

Cytogenetic and molecular analysis in Angelman syndrome.

Zackowski JL, Nicholls RD, Gray BA, Bent-Williams A, Gottlieb W, Harris PJ, Waters MF, Driscoll DJ, Zori RT, Williams CA. Zackowski JL, et al. Am J Med Genet. 1993 Apr 1;46(1):7-11. doi: 10.1002/ajmg.1320460104. Am J Med Genet. 1993. PMID: 8098583

7

Trisomy 1q42qter "syndrome": additional case report.

Storto P, Zackowski J, Leichtman L, Montgomery T, Newlin A. Storto P, et al. Am J Med Genet. 2001 Mar 15;99(3):258-9. doi: 10.1002/1096-8628(2001)9999:9999<::aid-ajmg1149>3.0.co;2-n. Am J Med Genet. 2001. PMID: 11241501 No abstract available.

8

Clinical, cytogenetic, and molecular evidence for an infant with Smith-Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletion.

Zori RT, Lupski JR, Heju Z, Greenberg F, Killian JM, Gray BA, Driscoll DJ, Patel PI, Zackowski JL. Zori RT, et al. Among authors: zackowski jl. Am J Med Genet. 1993 Sep 15;47(4):504-11. doi: 10.1002/ajmg.1320470414. Am J Med Genet. 1993. PMID: 8256814

9

Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p.

Leichtman LG, Zackowski JL, Storto PD, Newlin A. Leichtman LG, et al. Among authors: zackowski jl. Am J Med Genet. 1996 Jun 14;63(3):434-7. doi: 10.1002/(SICI)1096-8628(19960614)63:3<434::AID-AJMG4>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8737648

10

Molecular and cytogenetic analysis of familial Xp deletions.

Wandstrat AE, Conroy JM, Zurcher VL, Pasztor LM, Clark BA, Zackowski JL, Schwartz S. Wandstrat AE, et al. Among authors: zackowski jl. Am J Med Genet. 2000 Sep 11;94(2):163-9. doi: 10.1002/1096-8628(20000911)94:2<163::aid-ajmg9>3.0.co;2-u. Am J Med Genet. 2000. PMID: 10982973

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