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Items: 10

1.

Molecular characterization of a ring chromosome 16 from a patient with bilateral cataracts.

He W, Tuck-Muller CM, Martínez JE, Li S, Rowley ER, Wertelecki W.

Am J Med Genet. 2002 Jan 1;107(1):12-7.

PMID:
11807861
2.

Do human chromosomal bands 16p13 and 22q11-13 share ancestral origins?

Giles RH, Dauwerse HG, van Ommen GJ, Breuning MH.

Am J Hum Genet. 1998 Oct;63(4):1240-2. No abstract available.

3.
4.

Abnormality of chromosome 16 and its phenotypic expression.

Golden NL, Bilenker R, Johnson WE, Tischfield JA.

Clin Genet. 1981 Jan;19(1):41-5.

PMID:
7460380
5.

[Association of male XX with Pierre Robin syndrome in a child whose father has a balanced 46XY, t (16; 17) (p13;q21) translocation].

Petrus M, Bourrouillou G, Dutau G, Colombies P, Rochiccioli P.

J Genet Hum. 1981 Jun;29(2):191-6. French.

PMID:
7199077
6.

Different inducibility and possible significance of several concomitant "fragile sites" in two brothers.

Shabtai F, Orlin J, Hart J, Halbrecht I, Klar D, Friedman J.

Hum Genet. 1986 Sep;74(1):85-9.

PMID:
3019870
8.

Developmental delay, short stature, and minor facial anomalies in a child with ring chromosome 16.

Chodirker BN, Ray M, McAlpine PJ, Riordan D, Vust A, Pugh D, Chudley AE.

Am J Med Genet. 1988 Sep;31(1):145-51.

PMID:
2464927
10.

Pericentric inversion of chromosome 16 in a large kindred: spectrum of morbidity and mortality in offspring.

Bianchi DW, Nicholls RD, Russell KA, Miller WA, Ellin M, Lage JM.

Am J Med Genet. 1992 Jul 15;43(5):791-5.

PMID:
1642263

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