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Items: 7

1.

Prenatal diagnosis of de novo (7;19)(q11.2;q13.3) translocation associated with a thick corpus callosum and Wilms tumor of the kidneys.

Cavicchioni O, Gomes DM, Leroy B, Vialard F, Hillion Y, Selva J, Ville Y.

Prenat Diagn. 2005 Oct;25(10):876-8.

PMID:
16193462
2.

Prenatal detection of trisomy for the entire long arm of chromosome 7.

Ndah BV, Stead JA, Brancazio LR, Hummel M, Wenger SL.

J Med Genet. 2000 Jul;37(7):551-3. No abstract available.

3.

Constitutional inversion of chromosome 7 and hematologic cancers.

Stanley WS, Burkett SS, Segel B, Quiery A, George B, Lobel J, Shah N.

Cancer Genet Cytogenet. 1997 Jul 1;96(1):46-9.

PMID:
9209470
4.

Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.

Hsu LY, Yu MT, Richkind KE, Van Dyke DL, Crandall BF, Saxe DF, Khodr GS, Mennuti M, Stetten G, Miller WA, Priest JH.

Prenat Diagn. 1996 Jan;16(1):1-28.

PMID:
8821848
5.

Deletion mapping of the beta-glucuronidase gene.

Allanson JE, Gemmill RM, Hecht BK, Johnsen S, Wenger DA.

Am J Med Genet. 1988 Mar;29(3):517-22.

PMID:
3376995
6.

Proximal interstitial deletion of 7q: a case report and review of the literature.

Zackowski JL, Raffel LJ, Blank CA, Schwartz S.

Am J Med Genet. 1990 Jul;36(3):328-32. Review.

PMID:
2194394

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