Ledbetter DH - Search Results

1

Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(Xpter-->Xq26.1::15p11-->15qter).

Scheuerle A, Zenger-Hain JL, Van Dyke DL, Ledbetter DH, Greenberg F, Shaffer LG. Scheuerle A, et al. Among authors: ledbetter dh. Am J Med Genet. 1995 May 8;56(4):403-8. doi: 10.1002/ajmg.1320560411. Am J Med Genet. 1995. PMID: 7604850

2

Interstitial deletion of chromosome 18[del(18)(q11.2q12.2 or q12.2q21.1].

Surh LC, Ledbetter DH, Greenberg F. Surh LC, et al. Among authors: ledbetter dh. Am J Med Genet. 1991 Oct 1;41(1):15-7. doi: 10.1002/ajmg.1320410105. Am J Med Genet. 1991. PMID: 1719812

3

Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13.

Pettigrew AL, Greenberg F, Caskey CT, Ledbetter DH. Pettigrew AL, et al. Among authors: ledbetter dh. Hum Genet. 1991 Aug;87(4):452-6. doi: 10.1007/BF00197167. Hum Genet. 1991. PMID: 1879832

4

Di George anomaly associated with a de novo Y;22 translocation resulting in monosomy del(22)(q11.2).

Lupski JR, Langston C, Friedman R, Ledbetter DH, Greenberg F. Lupski JR, et al. Among authors: ledbetter dh. Am J Med Genet. 1991 Aug 1;40(2):196-8. doi: 10.1002/ajmg.1320400214. Am J Med Genet. 1991. PMID: 1897574

5

Determination of the origin of nondisjunction in a 49,XXXXY male using hypervariable dinucleotide repeat sequences.

Huang TH, Greenberg F, Ledbetter DH. Huang TH, et al. Among authors: ledbetter dh. Hum Genet. 1991 Apr;86(6):619-20. doi: 10.1007/BF00201553. Hum Genet. 1991. PMID: 2026425

6

Prenatal diagnosis of deletion 17p13 associated with DiGeorge anomaly.

Greenberg F, Courtney KB, Wessels RA, Huhta J, Carpenter RJ, Rich DC, Ledbetter DH. Greenberg F, et al. Among authors: ledbetter dh. Am J Med Genet. 1988 Sep;31(1):1-4. doi: 10.1002/ajmg.1320310102. Am J Med Genet. 1988. PMID: 3066218

7

Cytogenetic findings in a prospective series of patients with DiGeorge anomaly.

Greenberg F, Elder FF, Haffner P, Northrup H, Ledbetter DH. Greenberg F, et al. Among authors: ledbetter dh. Am J Hum Genet. 1988 Nov;43(5):605-11. Am J Hum Genet. 1988. PMID: 3189331 Free PMC article.

8

Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to a terminal del(22q).

Herman GE, Greenberg F, Ledbetter DH. Herman GE, et al. Among authors: ledbetter dh. Am J Med Genet. 1988 Apr;29(4):909-15. doi: 10.1002/ajmg.1320290423. Am J Med Genet. 1988. PMID: 3400736

9

Duplication of proximal 15q as a cause of Prader-Willi syndrome.

Pettigrew AL, Gollin SM, Greenberg F, Riccardi VM, Ledbetter DH. Pettigrew AL, et al. Among authors: ledbetter dh. Am J Med Genet. 1987 Dec;28(4):791-802. doi: 10.1002/ajmg.1320280403. Am J Med Genet. 1987. PMID: 3688017

10

Deletions of proximal 15q without Prader-Willi syndrome.

Greenberg F, Ledbetter DH. Greenberg F, et al. Among authors: ledbetter dh. Am J Med Genet. 1987 Dec;28(4):813-20. doi: 10.1002/ajmg.1320280405. Am J Med Genet. 1987. PMID: 3688019

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