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Items: 7

1.

[Increase of the LDH-B activity in a boy with 12p trisomy by malsegregation of a maternal translocation t(12;14) (q12;p11)].

Rethoré MO, Kaplan JC, Junien C, Cruveiller J, Dutrillaux B, Aurias A, Carpentier S, Lafourcade J, Lejeune.

Ann Genet. 1975 Jun;18(2):81-7. French.

PMID:
1081369
2.

Trisomy 20q caused by der(4) t(4;20) (q35;q13.1): report of a new patient and review of the literature.

Plotner PL, Smith JL, Northrup H.

Am J Med Genet. 2002 Jul 22;111(1):71-5. Review.

PMID:
12124739
3.

Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literature.

Taysi K, Chao WT, Monaghan N, Monaco MP.

Ann Genet. 1983;26(4):243-6. Review.

PMID:
6364954
4.

Interstitial deletion of the short arm of chromosome 12. Report of a new patient and review of the literature.

Fryns JP, Kleczkowska A, Van den Berghe H.

Ann Genet. 1990;33(1):43-5. Review.

PMID:
2195980
5.

9q34.3 deletion syndrome in three unrelated children.

Iwakoshi M, Okamoto N, Harada N, Nakamura T, Yamamori S, Fujita H, Niikawa N, Matsumoto N.

Am J Med Genet A. 2004 Apr 30;126A(3):278-83. Review.

PMID:
15054842
6.

Partial trisomy 8q. Two case reports with maternal translocation and inverted insertion: phenotype analyses and reflections on the risk.

Stengel-Rutkowski S, Lohse K, Herzog C, Apacik C, Couturier J, Albert A, Belohradsky B.

Clin Genet. 1992 Oct;42(4):178-85. Review.

PMID:
1424241
7.

Further delineation of 7p trisomy. Case report and review of literature.

Pallotta R, Dalprà L, Fusilli P, Zuffardi O.

Ann Genet. 1996;39(3):152-8. Review.

PMID:
8839888
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