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Results: 11

PubMed Links for Books (Select 2981620)

1.

Mosaic maternal uniparental isodisomy for chromosome 7q21-qter.

Reboul MP, Tandonnet O, Biteau N, Belet-de Putter C, Rebouissoux L, Moradkhani K, Vu PY, Saura R, Arveiler B, Lacombe D, Taine L, Iron A.

Clin Genet. 2006 Sep;70(3):207-13.

PMID:
16922723
2.

Familial reciprocal translocation t(7;16) associated with maternal uniparental disomy 7 in a Silver-Russell patient.

Dupont JM, Cuisset L, Cartigny M, Le Tessier D, Vasseur C, Rabineau D, Jeanpierre M.

Am J Med Genet. 2002 Sep 1;111(4):405-8.

PMID:
12210300
4.
5.

Paracentric inversions in man.

Madan K, Seabright M, Lindenbaum RH, Bobrow M.

J Med Genet. 1984 Dec;21(6):407-12. Review.

7.

The phenotype of partial dup(7q) reconsidered: a report of five new cases.

Forabosco A, Baroncini A, Dalpra L, Chessa L, Giannotti A, Maccagnani F, Dallapiccola B.

Clin Genet. 1988 Jul;34(1):48-59.

PMID:
3409538
8.

Cytogenetic analysis of 400 sperm from three translocation heterozygotes.

Martin RH, Barclay L, Hildebrand K, Ko E, Fowlow SB.

Hum Genet. 1990 Nov;86(1):33-9.

PMID:
2253936
9.

Interstitial deletion of the long arm of chromosome no. 7 (7q-) in an infant with multiple anomalies.

Higginson G, Weaver DD, Magenis RE, Prescott GH, Haag C, Hepburn DJ.

Clin Genet. 1976 Nov;10(5):307-12.

PMID:
991439
10.

[Interstitial deletion of the long arm of chromosome 7 in a female child with leprechaunism].

Ayraud N, Rovinski J, Lambert JC, Galiana A.

Ann Genet. 1976 Dec;19(4):265-8. French.

PMID:
797303
11.

Systematic analysis of 95 reciprocal translocations of autosomes.

Aurias A, Prieur M, Dutrillaux B, Lejeune J.

Hum Genet. 1978 Dec 29;45(3):259-82.

PMID:
738728
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