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Items: 7

1.

Subtle trisomy 12q24.3 and subtle monosomy 22q13.3: three new cases and review.

Rodríguez L, Martínez Guardia N, Herens C, Jamar M, Verloes A, López F, Santos Muñoz J, Martínez-Frías ML.

Am J Med Genet A. 2003 Oct 1;122A(2):119-24.

PMID:
12955763
2.

Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.

Riegel M, Baumer A, Jamar M, Delbecque K, Herens C, Verloes A, Schinzel A.

Hum Genet. 2001 Sep;109(3):286-94.

PMID:
11702209
3.

Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics.

Tönnies H, Stumm M, Wegner RD, Chudoba I, Kalscheuer V, Neitzel H.

Cytogenet Cell Genet. 2001;93(3-4):188-94.

PMID:
11528111
4.

Chromosomal aberrations in couples undergoing intracytoplasmic sperm injection: influence on implantation and ongoing pregnancy rates.

Scholtes MC, Behrend C, Dietzel-Dahmen J, van Hoogstraten DG, Marx K, Wohlers S, Verhoeven H, Zeilmaker GH.

Fertil Steril. 1998 Nov;70(5):933-7.

PMID:
9806579
5.

An unusual translocation between 12tel and 14q11 in a large kindred.

Palanduz S, Ustek D, Karaman B, Oztürk S, Cefle K, Başaran S.

Hereditas. 1998;128(3):231-4.

6.

Dissociation of a t(12;21) resulting in a normal cell line in two trisomic 21 sons of a nonmosaic t(12;21) father?

Juberg RC, Stallard R, Mowrey P, Valido CL.

Hum Genet. 1983;64(3):216-21.

PMID:
6224735
7.

Sperm chromosome analysis in a man heterozygous for a reciprocal translocation 46,XY t(12;20)(q24.3;q11).

Martin RH, McGillivray B, Barclay L, Hildebrand K, Ko E.

Hum Reprod. 1990 Jul;5(5):606-9.

PMID:
2394792

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