Incidence of 15q11q13 deletions in spermatozoa from Prader-Willi syndrome fathers

O. Molina; E. Anton; J. Blanco

Incidence of 15q11q13 deletions in spermatozoa from Prader-Willi syndrome fathers

O. Molina, E. Anton, J. Blanco

Department of Cellular Biology, Physiology and Immunology

Research output: Contribution to journal › Article › Research › peer-review

Original language	English
Journal	Chromosome Research
Publication status	Published - 2007

Cite this

TY - JOUR

T1 - Incidence of 15q11q13 deletions in spermatozoa from Prader-Willi syndrome fathers

AU - Molina, O.

AU - Anton, E.

AU - Blanco, J.

PY - 2007

Y1 - 2007

UR - http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000248859800154&KeyUID=WOS:000248859800154

M3 - Article

SN - 0967-3849

JO - Chromosome Research

JF - Chromosome Research

ER -

Incidence of 15q11q13 deletions in spermatozoa from Prader-Willi syndrome fathers

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