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Results: 5

PubMed Links for Books (Select 2982910)

1.

Prenatal and postnatal characterization of a de novo Xq22.1 terminal deletion.

Vaglio A, Greif G, Bernal M, Sanguinetti C, Mechoso B, Quadrelli A, Tucci P, Milunsky JM, Huang XL, Pagano S, Quadrelli R.

Genet Test. 2006 Winter;10(4):272-6.

PMID:
17253933
2.
3.

De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype.

Tihy F, Lemyre E, Lemieux N, Dallaire L.

Am J Med Genet. 1999 Dec 3;87(4):302-5. Review.

PMID:
10588834
4.

Three patients with a 45,X/46,X,psu dic(Xp) karyotype.

Dalton P, Coppin B, James R, Skuse D, Jacobs P.

J Med Genet. 1998 Jun;35(6):519-24. Review.

5.

Molecular cytogenetic identification of four X chromosome duplications.

Zhang A, Weaver DD, Palmer CG.

Am J Med Genet. 1997 Jan 10;68(1):29-38. Review.

PMID:
8986272
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