Erickson RP - Search Results

1

True hermaphroditism with partial duplication of chromosome 22 and without SRY.

Aleck KA, Argueso L, Stone J, Hackel JG, Erickson RP. Aleck KA, et al. Among authors: erickson rp. Am J Med Genet. 1999 Jul 2;85(1):2-4. doi: 10.1002/(sici)1096-8628(19990702)85:1<2::aid-ajmg2>3.0.co;2-g. Am J Med Genet. 1999. PMID: 10377005

2

Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy.

Cassidy SB, Lai LW, Erickson RP, Magnuson L, Thomas E, Gendron R, Herrmann J. Cassidy SB, et al. Among authors: erickson rp. Am J Hum Genet. 1992 Oct;51(4):701-8. Am J Hum Genet. 1992. PMID: 1357962 Free PMC article.

3

An amino acid change in the DNA-binding region of Sry, found in Mus musculus domesticus and other species, does not explain C57BL/6J-YDOM sex-reversal.

Graves PE, Erickson RP. Graves PE, et al. Among authors: erickson rp. Biochem Biophys Res Commun. 1992 May 29;185(1):310-6. doi: 10.1016/s0006-291x(05)90001-6. Biochem Biophys Res Commun. 1992. PMID: 1599466

4

Detection of circular and linear transcripts of Sry in pre-implantation mouse embryos: differences in requirement for reverse transcriptase.

Boyer TR, Erickson RP. Boyer TR, et al. Among authors: erickson rp. Biochem Biophys Res Commun. 1994 Jan 28;198(2):492-6. doi: 10.1006/bbrc.1994.1072. Biochem Biophys Res Commun. 1994. PMID: 7507663

5

Transcription of circular and noncircular forms of Sry in mouse testes.

Zwingman T, Fujimoto H, Lai LW, Boyer T, Ao A, Stalvey JR, Blecher SR, Erickson RP. Zwingman T, et al. Among authors: erickson rp. Mol Reprod Dev. 1994 Apr;37(4):370-81. doi: 10.1002/mrd.1080370403. Mol Reprod Dev. 1994. PMID: 7516683

6

A "balanced" Y;16 translocation associated with Turner-like neonatal lymphedema suggests the location of a potential anti-Turner gene on the Y chromosome.

Erickson RP, Hudgins L, Stone JF, Schmidt S, Wilke C, Glover TW. Erickson RP, et al. Cytogenet Cell Genet. 1995;71(2):163-7. doi: 10.1159/000134099. Cytogenet Cell Genet. 1995. PMID: 7656589

7

Sequence variation in the 5', putative promoter of Sry and its possible relevance to the C57BL/6J-YDOM sex reversal.

Graves PE, Erickson RP. Graves PE, et al. Among authors: erickson rp. Biochem Biophys Res Commun. 1995 Mar 17;208(2):624-8. doi: 10.1006/bbrc.1995.1384. Biochem Biophys Res Commun. 1995. PMID: 7695616

8

SRY alone can induce normal male sexual differentiation.

López M, Torres L, Méndez JP, Cervantes A, Alfaro G, Pérez-Palacios G, Erickson RP, Kofman-Alfaro S. López M, et al. Among authors: erickson rp. Am J Med Genet. 1995 Jan 30;55(3):356-8. doi: 10.1002/ajmg.1320550321. Am J Med Genet. 1995. PMID: 7726236

9

Pulmonary atresia associated with maternal 22q11.2 deletion: possible parent of origin effect in the conotruncal anomaly face syndrome.

Seaver LH, Pierpont JW, Erickson RP, Donnerstein RL, Cassidy SB. Seaver LH, et al. Among authors: erickson rp. J Med Genet. 1994 Nov;31(11):830-4. doi: 10.1136/jmg.31.11.830. J Med Genet. 1994. PMID: 7853364 Free PMC article.

10

Female pseudohermaphroditism with multiple caudal anomalies: absence of Y-specific DNA sequences as pathogenetic factors.

Seaver LH, Grimes J, Erickson RP. Seaver LH, et al. Among authors: erickson rp. Am J Med Genet. 1994 May 15;51(1):16-21. doi: 10.1002/ajmg.1320510105. Am J Med Genet. 1994. PMID: 7913293

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