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• W2022308283 abstract "American Journal of Medical GeneticsVolume 69, Issue 1 p. 96-97 Full Access A case revisited: Recent presentation of incontinentia pigmenti in association with a previously reported X;autosome translocation Tamison Jewett, Corresponding Author Tamison Jewett Department of Pediatrics, Section on Medical Genetics, Bowman Gray School of Medicine of Wake Forest University Medical Center, Winston-Salem, North CarolinaDepartment of Pediatrics, Section on Medical Genetics, Bowman Gray School of Medicine of Wake Forest University, Medical Center Drive, Winston-Salem, NC 27157Search for more papers by this authorP. Suzanne Hart, P. Suzanne Hart Department of Pediatrics, Section on Medical Genetics, Bowman Gray School of Medicine of Wake Forest University Medical Center, Winston-Salem, North CarolinaSearch for more papers by this authorP. Nagesh Rao, P. Nagesh Rao Department of Pediatrics, Section on Medical Genetics, Bowman Gray School of Medicine of Wake Forest University Medical Center, Winston-Salem, North CarolinaSearch for more papers by this authorMark J. Pettenati, Mark J. Pettenati Department of Pediatrics, Section on Medical Genetics, Bowman Gray School of Medicine of Wake Forest University Medical Center, Winston-Salem, North CarolinaSearch for more papers by this author Tamison Jewett, Corresponding Author Tamison Jewett Department of Pediatrics, Section on Medical Genetics, Bowman Gray School of Medicine of Wake Forest University Medical Center, Winston-Salem, North CarolinaDepartment of Pediatrics, Section on Medical Genetics, Bowman Gray School of Medicine of Wake Forest University, Medical Center Drive, Winston-Salem, NC 27157Search for more papers by this authorP. Suzanne Hart, P. Suzanne Hart Department of Pediatrics, Section on Medical Genetics, Bowman Gray School of Medicine of Wake Forest University Medical Center, Winston-Salem, North CarolinaSearch for more papers by this authorP. Nagesh Rao, P. Nagesh Rao Department of Pediatrics, Section on Medical Genetics, Bowman Gray School of Medicine of Wake Forest University Medical Center, Winston-Salem, North CarolinaSearch for more papers by this authorMark J. Pettenati, Mark J. Pettenati Department of Pediatrics, Section on Medical Genetics, Bowman Gray School of Medicine of Wake Forest University Medical Center, Winston-Salem, North CarolinaSearch for more papers by this author First published: 06 December 1998 https://doi.org/10.1002/(SICI)1096-8628(19970303)69:1<96::AID-AJMG18>3.0.CO;2-JCitations: 5AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. References Bitoun P, Philippe C, Cherif M, Mulcahy M-T, Gilgenkrantz S (1992): Incontinentia pigmenti (type 1) and X;5 translocation. Ann Génét 35: 51–54. Cannizzaro LA, Hecht F (1987): Gene for incontinentia pigmenti maps to band Xp11 with an (X;10)(p11;q22) translocation. Clin Genet 32: 66–69. Crolla JA, Gilgenkrantz S, de Grouchy J, Kajii T, Bobrow M (1989): Incontinentia pigmenti and X-autosome translocation: Non-isotopic in situ hybridization with and X-centromeric-specific probe (pSV2X5) reveals a possible X-centromeric breakpoint in one of five published cases. Hum Genet 81: 269–272. deGrouchy J, Turleau C, Doussau de Bazignan M, Maroteaux P, Thibaud D (1985): Incontinentia pigmenti (IP) and r(X): tentative mapping of the IP locus to the X juxtacentromeric region. Ann Génét 28: 86–89. Gilgenkrantz S, Tridon P, Pinel-Briquel N, Beurey J, Weber M (1985): Translocation (X;9)(p11;q34) in a girl with incontinentia pigmenti (IP): Implications for the regional assignment of the IP locus to Xp11? Ann Génét 26: 90–92. Hodgson SV, Neville B, Jones Rwa, Fear C, Bobrow M (1985): Two cases of X/autosome translocation in females with incontinentia pigmenti. Hum Genet 71: 231–234. Kajii T, Tsukahara M, Fukushima U, Hata A, Matsuo K, Kuroki Y (1985): Translocation (X;13)(p11.2;q12.3) in a girl with incontinentia pigmenti and bilateral retinoblastoma. Ann Génét 28: 219–223. Pettenati MJ, Teot LA, Smith C, Hayworth R, Thomas IT, Veille JC, Rao N (1993): Unbalanced mosaic karyotypes with different structural abnormalities involving a common chromosome region: Report of 2 cases. Am J Med Genet 45: 365–369. Citing Literature Volume69, Issue13 March 1997Pages 96-97 ReferencesRelatedInformation" @default.
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• W2022308283 title "A case revisited: Recent presentation of incontinentia pigmenti in association with a previously reported X;autosome translocation" @default.
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