Stratton RF - Search Results

1

Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly.

Dobyns WB, Stratton RF, Greenberg F. Dobyns WB, et al. Among authors: stratton rf. Am J Med Genet. 1984 Jul;18(3):509-26. doi: 10.1002/ajmg.1320180320. Am J Med Genet. 1984. PMID: 6476009

2

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: stratton rf. Am J Med Genet. 1986 Apr;23(4):853-9. doi: 10.1002/ajmg.1320230402. Am J Med Genet. 1986. PMID: 3963054

3

New chromosomal syndrome: Miller-Dieker syndrome and monosomy 17p13.

Stratton RF, Dobyns WB, Airhart SD, Ledbetter DH. Stratton RF, et al. Hum Genet. 1984;67(2):193-200. doi: 10.1007/BF00273000. Hum Genet. 1984. PMID: 6745939

4

Miller-Dieker syndrome: lissencephaly and monosomy 17p.

Dobyns WB, Stratton RF, Parke JT, Greenberg F, Nussbaum RL, Ledbetter DH. Dobyns WB, et al. Among authors: stratton rf. J Pediatr. 1983 Apr;102(4):552-8. doi: 10.1016/s0022-3476(83)80183-8. J Pediatr. 1983. PMID: 6834189

5

Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.

Stratton RF, Dobyns WB, Greenberg F, DeSana JB, Moore C, Fidone G, Runge GH, Feldman P, Sekhon GS, Pauli RM, et al. Stratton RF, et al. Am J Med Genet. 1986 Jul;24(3):421-32. doi: 10.1002/ajmg.1320240305. Am J Med Genet. 1986. PMID: 3728561

6

Cobblestone lissencephaly with normal eyes and muscle.

Dobyns WB, Patton MA, Stratton RF, Mastrobattista JM, Blanton SH, Northrup H. Dobyns WB, et al. Among authors: stratton rf. Neuropediatrics. 1996 Apr;27(2):70-5. doi: 10.1055/s-2007-973752. Neuropediatrics. 1996. PMID: 8737821

7

Pallister-Killian and Fryns syndromes.

Stratton RF, Moore CM, Popham CS, DuPont BR, Mattern VL. Stratton RF, et al. Am J Med Genet. 1994 May 15;51(1):90. doi: 10.1002/ajmg.1320510124. Am J Med Genet. 1994. PMID: 8030681 No abstract available.

8

An additional case of deletion 17p11.2.

Popp DW, Johnson CP, Stratton RF. Popp DW, et al. Among authors: stratton rf. Am J Med Genet. 1987 Feb;26(2):493-5. doi: 10.1002/ajmg.1320260228. Am J Med Genet. 1987. PMID: 3812598 No abstract available.

9

Deletion 5q35.3.

Stratton RF, Tedrowe NA, Tolworthy JA, Patterson RM, Ryan SG, Young RS. Stratton RF, et al. Am J Med Genet. 1994 Jun 1;51(2):150-2. doi: 10.1002/ajmg.1320510214. Am J Med Genet. 1994. PMID: 8092192

10

Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.

DuPont BR, Huff RW, Ridgway LE, Stratton RF, Moore CM. DuPont BR, et al. Among authors: stratton rf. Am J Med Genet. 1994 Mar 1;50(1):21-7. doi: 10.1002/ajmg.1320500105. Am J Med Genet. 1994. PMID: 8160748 Review.

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