Greenberg F - Search Results

1

Behavioral phenotype of Smith-Magenis syndrome (del 17p11.2).

Smith AC, Dykens E, Greenberg F. Smith AC, et al. Among authors: greenberg f. Am J Med Genet. 1998 Mar 28;81(2):179-85. doi: 10.1002/(sici)1096-8628(19980328)81:2<179::aid-ajmg10>3.0.co;2-e. Am J Med Genet. 1998. PMID: 9613859 Review.

2

Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder.

Grimbacher B, Holland SM, Gallin JI, Greenberg F, Hill SC, Malech HL, Miller JA, O'Connell AC, Puck JM. Grimbacher B, et al. Among authors: greenberg f. N Engl J Med. 1999 Mar 4;340(9):692-702. doi: 10.1056/NEJM199903043400904. N Engl J Med. 1999. PMID: 10053178 Free article.

3

Sleep disturbance in Smith-Magenis syndrome (del 17 p11.2).

Smith AC, Dykens E, Greenberg F. Smith AC, et al. Among authors: greenberg f. Am J Med Genet. 1998 Mar 28;81(2):186-91. Am J Med Genet. 1998. PMID: 9613860

4

Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.

Mutirangura A, Greenberg F, Butler MG, Malcolm S, Nicholls RD, Chakravarti A, Ledbetter DH. Mutirangura A, et al. Among authors: greenberg f. Hum Mol Genet. 1993 Feb;2(2):143-51. doi: 10.1093/hmg/2.2.143. Hum Mol Genet. 1993. PMID: 8499903 Free PMC article.

5

Ophthalmic manifestations of Smith-Magenis syndrome.

Chen RM, Lupski JR, Greenberg F, Lewis RA. Chen RM, et al. Among authors: greenberg f. Ophthalmology. 1996 Jul;103(7):1084-91. doi: 10.1016/s0161-6420(96)30563-0. Ophthalmology. 1996. PMID: 8684798 Review.

6

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: greenberg f. Am J Med Genet. 1991 Aug 1;40(2):196-8. doi: 10.1002/ajmg.1320400214. Am J Med Genet. 1991. PMID: 1897574

7

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: greenberg f. Am J Med Genet. 1991 Oct 1;41(1):15-7. doi: 10.1002/ajmg.1320410105. Am J Med Genet. 1991. PMID: 1719812

8

Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patients.

Trask BJ, Mefford H, van den Engh G, Massa HF, Juyal RC, Potocki L, Finucane B, Abuelo DN, Witt DR, Magenis E, Baldini A, Greenberg F, Lupski JR, Patel PI. Trask BJ, et al. Among authors: greenberg f. Hum Genet. 1996 Dec;98(6):710-8. doi: 10.1007/s004390050291. Hum Genet. 1996. PMID: 8931707

9

Clinical and molecular evaluation of four patients with partial duplications of the long arm of chromosome 18.

Mewar R, Kline AD, Harrison W, Rojas K, Greenberg F, Overhauser J. Mewar R, et al. Among authors: greenberg f. Am J Hum Genet. 1993 Dec;53(6):1269-78. Am J Hum Genet. 1993. PMID: 8250043 Free PMC article. Review.

10

Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17.

Greenberg F, Stratton RF, Lockhart LH, Elder FF, Dobyns WB, Ledbetter DH. Greenberg F, et al. Am J Med Genet. 1986 Apr;23(4):853-9. doi: 10.1002/ajmg.1320230402. Am J Med Genet. 1986. PMID: 3963054

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