Chromosome 16 Abnormalities in Embryos and in Sperm from a Male with a Fragile Site at 16q22.1

Publisher： Karger

E-ISSN： 1424-859x|142|2|134-139

ISSN： 1424-8581

Source： Cytogenetic and Genome Research, Vol.142, Iss.2, 2014-01, pp. : 134-139

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Chromosome Breakage in Human Preimplantation Embryos from Carriers of Structural Chromosomal Abnormalities in Relation to Fragile Sites, Maternal Age, and Poor Sperm Factors

Cytogenetic and Genome Research, Vol. 136, Iss. 1, 2011-12 ,pp. : 21-29

Karger

Access to resources Recommend Favorite

The rare human fragile site 16B

Cytogenetic and Genome Research, Vol. 100, Iss. 1-4, 2003-10 ,pp. : 85-88

Karger

Access to resources Recommend Favorite

Assignment¹ of the E-cadherin gene (CDH1) to chromosome 16q22.1 by radiation hybrid mapping

Cytogenetic and Genome Research, Vol. 83, Iss. 1-2, 1999-02 ,pp. : 82-83

Karger

Access to resources Recommend Favorite

Assignment¹ of E-cadherin (CDH1) and KSP-cadherin (CDH16) to chromosome 16q22.1 by radiation hybrid mapping

Cytogenetic and Genome Research, Vol. 88, Iss. 3-4, 2000-05 ,pp. : 253-254

Karger

Access to resources Recommend Favorite

Distal Partial Trisomy 15q26 and Partial Monosomy 16p13.3 in a 36-Year-Old Male with Clinical Features of Both Chromosomal Abnormalities

Cytogenetic and Genome Research, Vol. 145, Iss. 1, 2015-04 ,pp. : 29-34

Karger

Access to resources Recommend Favorite