Elder FF - Search Results

1

Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4.

Altherr MR, Bengtsson U, Elder FF, Ledbetter DH, Wasmuth JJ, McDonald ME, Gusella JF, Greenberg F. Altherr MR, et al. Among authors: elder ff. Am J Hum Genet. 1991 Dec;49(6):1235-42. Am J Hum Genet. 1991. PMID: 1746553 Free PMC article.

2

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: elder ff. Am J Hum Genet. 1988 Nov;43(5):605-11. Am J Hum Genet. 1988. PMID: 3189331 Free PMC article.

3

Isodicentric X chromosome in a patient with Turner syndrome--implications for localization of the X-inactivation center.

Pettigrew AL, McCabe ER, Elder FF, Ledbetter DH. Pettigrew AL, et al. Among authors: elder ff. Hum Genet. 1991 Aug;87(4):498-502. doi: 10.1007/BF00197176. Hum Genet. 1991. PMID: 1879836

4

Neonatal diagnosis of Prader-Willi syndrome and its implications.

Greenberg F, Elder FF, Ledbetter DH. Greenberg F, et al. Among authors: elder ff. Am J Med Genet. 1987 Dec;28(4):845-56. doi: 10.1002/ajmg.1320280409. Am J Med Genet. 1987. PMID: 3688023

5

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. Among authors: elder ff. Am J Med Genet. 1986 Apr;23(4):853-9. doi: 10.1002/ajmg.1320230402. Am J Med Genet. 1986. PMID: 3963054

6

Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.

Shapira SK, McCaskill C, Northrup H, Spikes AS, Elder FF, Sutton VR, Korenberg JR, Greenberg F, Shaffer LG. Shapira SK, et al. Among authors: elder ff. Am J Hum Genet. 1997 Sep;61(3):642-50. doi: 10.1086/515520. Am J Hum Genet. 1997. PMID: 9326330 Free PMC article.

7

45,X/46,X,+r(X) can have a distinct phenotype different from Ullrich-Turner syndrome.

Grompe M, Rao N, Elder FF, Caskey CT, Greenberg F. Grompe M, et al. Among authors: elder ff. Am J Med Genet. 1992 Jan 1;42(1):39-43. doi: 10.1002/ajmg.1320420110. Am J Med Genet. 1992. PMID: 1339199

8

Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism.

Christian SL, Smith AC, Macha M, Black SH, Elder FF, Johnson JM, Resta RG, Surti U, Suslak L, Verp MS, Ledbetter DH. Christian SL, et al. Among authors: elder ff. Prenat Diagn. 1996 Apr;16(4):323-32. doi: 10.1002/(SICI)1097-0223(199604)16:4<323::AID-PD856>3.0.CO;2-5. Prenat Diagn. 1996. PMID: 8734806

9

Unbalanced translocation (15;17)(q13;13.3) with apparent Prader-Willi syndrome but without Miller-Dieker syndrome.

Elder FF, Nichols MM, Hood OJ, Harrison WR 3rd. Elder FF, et al. Am J Med Genet. 1985 Mar;20(3):519-24. doi: 10.1002/ajmg.1320200312. Am J Med Genet. 1985. PMID: 3993677

10

Identical twins with deletion 16q syndrome: evidence that 16q12.2-q13 is the critical band region.

Elder FF, Ferguson JW, Lockhart LH. Elder FF, et al. Hum Genet. 1984;67(2):233-6. doi: 10.1007/BF00273010. Hum Genet. 1984. PMID: 6540242

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