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Items: 18

1.

Trisomy 2 mosaicism in hypomelanosis of Ito.

Gupta S, Shah S, Mcgaw A, Mercado T, Zaslav AL, Tegay D.

Am J Med Genet A. 2007 Oct 15;143A(20):2466-8. No abstract available.

PMID:
17853474
2.

[Hypomelanosis of Ito in a girl with Trisomy 13 mosaicism: a cytogenetic study].

Ronger S, Till M, Kanitakis J, Balme B, Thomas L.

Ann Dermatol Venereol. 2003 Nov;130(11):1033-8. Review. French.

PMID:
14724538
3.

Partial trisomy 10 mosaicism with cutaneous manifestations: report of a case and review of the literature.

Boon C, Markello T, Jackson-Cook C, Pandya A.

Clin Genet. 1996 Nov;50(5):417-21. Review.

PMID:
9007335
4.

Trisomy 20 mosaicism in two unrelated girls with skin hypopigmentation and normal intellectual development.

Baty BJ, Olson SB, Magenis RE, Carey JC.

Am J Med Genet. 2001 Mar 15;99(3):210-6. Review.

PMID:
11241492
5.

Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes.

Taibjee SM, Bennett DC, Moss C.

Br J Dermatol. 2004 Aug;151(2):269-82. Review.

PMID:
15327534
6.

Linear hypopigmentation and hyperpigmentation, including mosaicism.

Loomis CA.

Semin Cutan Med Surg. 1997 Mar;16(1):44-53. Review.

PMID:
9125765
7.

Mosaic tetrasomy 13q and phylloid hypomelanosis: a case report and review of the literature.

Myers JN Jr, Davis L, Sheehan D, Kulharya AS.

Pediatr Dermatol. 2015 Mar-Apr;32(2):263-6. doi: 10.1111/pde.12375. Epub 2014 Jun 12. Review.

PMID:
24920397
8.

Tumors and hypomelanosis of Ito.

Ruggieri M, Magro G, Ruggieri M, Polizzi A.

Arch Pathol Lab Med. 2001 May;125(5):599-601. Review. No abstract available.

PMID:
11339219
9.

Is trisomy 14 mosaic a clinically recognizable syndrome?--case report and review.

von Sneidern E, Lacassie Y.

Am J Med Genet A. 2008 Jun 15;146A(12):1609-13. doi: 10.1002/ajmg.a.32334. Review. No abstract available.

PMID:
18449929
10.

Trisomy 14 Mosaicism: a case without evidence of neurodevelopmental delay and a review of the literature.

Merritt TA, Natarajan G.

Am J Perinatol. 2007 Oct;24(9):563-6. Epub 2007 Sep 24. Review.

PMID:
17893842
11.

An unusual association of pigmentary mosaicism (hypomelanosis of Ito) with generalized hypertrichosis.

Khandpur S, Minz A, Sharma VK.

Clin Exp Dermatol. 2006 May;31(3):467-8. Review. No abstract available.

PMID:
16681611
12.

Fetal trisomy 5 mosaicism: case report and literature review.

Villa N, Redaelli S, Borroni C, Colombo C, Roncaglia N, Sala E, Crosti F, Cappellini A, Dalprà L.

Am J Med Genet A. 2007 Oct 1;143A(19):2343-6. Review. No abstract available.

PMID:
17702005
13.

Colocalized nevus depigmentosus and lentigines with underlying breast hypoplasia: a case of reverse mutation?

Jagia R, Mendiratt V, Koranne RV, Sardana K, Bhushan P, Solanki RS.

Dermatol Online J. 2004 Jul 15;10(1):12. Review.

14.

Small supernumerary chromosome marker generating complete and pure trisomy 18p, characterized by molecular cytogenetic techniques and review.

Rodríguez L, Liehr T, Mrasek K, Mansilla E, Martínez-Fernández ML, Garcia A, Martínez-Frías ML.

Am J Med Genet A. 2007 Nov 15;143A(22):2727-32. Review.

PMID:
17937429
15.

Acquired trisomy 2 is not systematically associated with tumors.

Berger R.

Cancer Genet Cytogenet. 2004 Aug;153(1):86-7. Review. No abstract available.

PMID:
15325103
16.

Mosaicism for trisomy 21 in a patient with young-onset dementia: a case report and brief literature review.

Ringman JM, Rao PN, Lu PH, Cederbaum S.

Arch Neurol. 2008 Mar;65(3):412-5. doi: 10.1001/archneur.65.3.412. Review.

PMID:
18332257
17.

[Hypomelanosis of Ito, pigmentary dysplasia].

Kim KC.

Ryoikibetsu Shokogun Shirizu. 2001;(33):854-5. Review. Japanese. No abstract available.

PMID:
11462722
18.

Partial trisomy 19p13.3 and partial monosomy 1p36.3: Clinical report and a literature review.

Puvabanditsin S, Garrow E, Brandsma E, Savla J, Kunjumon B, Gadi I.

Am J Med Genet A. 2009 Aug;149A(8):1782-5. doi: 10.1002/ajmg.a.32972. Review.

PMID:
19610110

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