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Items: 10

1.

Lack of intraindividual variation of unbalanced spermatozoa frequencies from a 46,XY,t(9;22)(q21;q11.2) carrier: case report.

Morel F, Douet-Guilbert N, Le Bris MJ, Herry A, Marchetti C, Lefebvre V, Delobel B, Amice V, Amice J, De Braekeleer M.

Hum Reprod. 2004 Oct;19(10):2227-30. Epub 2004 Aug 6.

2.

Patient with trisomy 9p and a hypoplastic left heart with a tricentric chromosome 9.

Morrissette JJ, Laufer-Cahana A, Medne L, Russell KL, Venditti CP, Kline R, Zackai EH, Spinner NB.

Am J Med Genet A. 2003 Dec 15;123A(3):279-84.

PMID:
14608650
3.

Multicolor karyotypic interpretation of a heterochromatin-associated marker chromosome in a dysmorphic girl with developmental delay.

Picker JD, Cox GF, Fan YS, Fowler DJ, Weremowicz S, Morton CC, Lee C.

Am J Med Genet. 2002 Jul 15;110(4):393-6. No abstract available.

PMID:
12116216
4.

Viability thresholds for partial trisomies and monosomies. A study of 1,159 viable unbalanced reciprocal translocations.

Cohen O, Cans C, Mermet MA, Demongeot J, Jalbert P.

Hum Genet. 1994 Feb;93(2):188-94. Review.

PMID:
8112744
5.

A case of tetrasomy 9p.

Andou R, Mimaki T, Ogihara T, Tamai H, Mino M.

Acta Paediatr Jpn. 1994 Dec;36(6):724-6.

PMID:
7532895
6.
7.

Precise identification of various chromosomal abnormalities.

Hirschhorn K, Lucas M, Wallace I.

Ann Hum Genet. 1973 Apr;36(4):375-9. No abstract available.

PMID:
4270654
8.

Maternal 3:1 disjunction in a translocation 9/17.

Sánchez Ferrer MA, de Torres ML, Abrisqueta JA.

Hum Genet. 1986 Jun;73(2):188. No abstract available.

PMID:
3721506
10.

Meiotic behavior of five human reciprocal translocations.

Chandley AC, Seuánez H, Fletcher JM.

Cytogenet Cell Genet. 1976;17(2):98-111. No abstract available.

PMID:
975939
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