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Items: 5

1.

Familial translocation t(3;10) (p26.3;p12.31) leading to trisomy 10p12.31-->pter and monosomy 3p26.3-->pter in seven members.

Nucaro AL, Meloni M, Pisano T, Melis P, Rossi E, Rossino R, Corona S, Loi M, Achena F, Zuffardi O, Cianchetti C.

Am J Med Genet A. 2008 Dec 15;146A(24):3242-5. doi: 10.1002/ajmg.a.32590. No abstract available.

PMID:
19012344
2.

Trisomy of 3pter in a patient with apparent C (trigonocephaly) syndrome.

McGaughran J, Aftimos S, Oei P.

Am J Med Genet. 2000 Oct 2;94(4):311-5.

PMID:
11038445
3.

Minute chromosomal rearrangements detected prenatally by fluorescence in situ hybridization.

Suzumori K, Tanemura M, Oya N, Suzumori N, Kim KC, Ohashi H, Fukushima Y.

Prenat Diagn. 1998 Jul;18(7):725-30.

PMID:
9706655
5.

Tuberous sclerosis in a child with de novo translocation t(3;12) (p26.3;q23.3).

Fahsold R, Rott HD, Claussen U, Schmalenberger B.

Clin Genet. 1991 Oct;40(4):326-8.

PMID:
1756605
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