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Items: 8

1.

The Haspeslagh syndrome (MIM 177980) is caused by an unbalanced reciprocal 6q/9p translocation.

Devriendt K, Holvoet M, De Mûelenaere A, Fryns JP.

Clin Genet. 2000 Jan;57(1):83-5. No abstract available.

PMID:
10733241
2.

Fish mapping of a translocation breakpoint at 6q21 (or q22) in a patient with heterotaxia.

Kato R, Matsumoto N, Fujimoto M, Nakano M, Nakamura Y, Niikawa N.

Jpn J Hum Genet. 1997 Dec;42(4):525-32.

PMID:
9560952
3.

[Familial observation of partial trisomy 6, and probable partial monosomy 18q by parental translocation].

D'Emma C, Crippa L, Delozier C, Michail E, Graber P.

J Genet Hum. 1982 Mar;30(1):39-50. French.

PMID:
7130955
4.

Prenatal diagnosis in 3,000 women for chromosome, X-linked, and metabolic disorders.

Daniel A, Stewart L, Saville T, Brookwell R, Paull H, Purvis-Smith S, Lam-Po-Tang PR.

Am J Med Genet. 1982 Jan;11(1):61-75.

PMID:
7065004
5.

Trisomy for the proximal segment of the long arm of chromosome 13: a new entity?

Escobar JI, Yunis JJ.

Am J Dis Child. 1974 Aug;128(2):221-2. No abstract available.

PMID:
4855264
6.

Partial trisomy 13: karyotype 46,XY,-6, plus t(13q,6q).

Fryns JP, Eggermont E, Verresen H, van den Berghe H.

Humangenetik. 1974 Jan 22;21(1):47-54. No abstract available.

PMID:
4837512
7.

Trisomy 12p due to familial t(12p-,6q plus) translocation.

Fryns JP, Van Den Berghe H.

Humangenetik. 1974;24(3):247-52. No abstract available.

PMID:
4140836
8.

An autosomal transcript in skeletal muscle with homology to dystrophin.

Love DR, Hill DF, Dickson G, Spurr NK, Byth BC, Marsden RF, Walsh FS, Edwards YH, Davies KE.

Nature. 1989 May 4;339(6219):55-8.

PMID:
2541343
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