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Results: 5

PubMed Links for Books (Select 2981262)

1.

Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).

Chen CP, Lin SP, Lin CC, Li YC, Chern SR, Chen WM, Lee CC, Hsieh LJ, Wang W.

Prenat Diagn. 2005 Feb;25(2):112-8. Review.

PMID:
15712324
2.

Inherited and de novo deletion of the tyrosine aminotransferase gene locus at 16q22.1----q22.3 in a patient with tyrosinemia type II.

Natt E, Westphal EM, Toth-Fejel SE, Magenis RE, Buist NR, Rettenmeier R, Scherer G.

Hum Genet. 1987 Dec;77(4):352-8.

PMID:
2891604
3.

A linkage group with FRA16B (the fragile site at 16q22.1).

Mulley JC, Hyland VJ, Fratini A, Bates LJ, Gedeon AK, Sutherland GR.

Hum Genet. 1989 May;82(2):131-3.

PMID:
2722188
4.
5.

Interstitial deletion of chromosome 16q: 16q22 is critical for 16q- syndrome.

Fujiwara M, Yoshimoto T, Morita Y, Kamada M.

Am J Med Genet. 1992 Jun 1;43(3):561-4.

PMID:
1605249
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