Holoprosencephaly
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Facial and brain anomalies in holoprosencephaly related chromosome aberrations characterized
news-medical.net — “Researchers at Signature Genomic Laboratories, which performs diagnostic genetic testing of chromosome abnormalities in individuals with unexplained physical and developmental disabilities, recently characterized a broad spectrum of facial and brain anomalies in individuals with chromosome aberrations associated with holoprosencephaly.” View full resource at news-medical.net
Most Recently Shared on January 27, 2010 at 6:34 pm By:
Genetics News: Facial and brain anomalies in holoprosencephaly related chromosome aberrations characterized: Resea... http://bit.ly/9eR96B
Researchers At Signature Genomics Attribute Diverse Spectrum Of Brain And Facial Anomalies To Genetic Regions Associated With Holoprosencephaly
medicalnewstoday.com — “Researchers at Signature Genomic Laboratories, which performs diagnostic genetic testing of chromosome abnormalities in individuals with unexplained physical and developmental disabilities, recent” View full resource at medicalnewstoday.com
Most Recently Shared on January 27, 2010 at 7:37 am By:
Researchers At Signature Genomics Attribute Diverse Spectrum Of Brain And Facial Anomalies To Genetic Regions Associa.. http://bit.ly/dcR2wA
Journal of Medical Case Reports | Abstract | Holoprosencephaly in an Egyptian baby with ectrodactyly-ectodermal dysplasia-cleft syndrome: a case report
jmedicalcasereports.com — “Ectrodactyly-ectodermal dysplasia-cleft lip or palate syndrome (OMIM No. 129900) is characterized by the triad of ectrodactyly, ectodermal dysplasia and facial clefting (of the lip and/or palate). Holoprosencephaly denotes a failure in the division of the embryonic forebrain (prosencephalon) into distinct lateral cerebral hemisphere. The association between ectrodactyly-ectodermal dysplasia-cleft lip or palate syndrome and holoprosencephaly is very rare. Here we report holoprosencephaly in an Eg” View full resource at jmedicalcasereports.com
Most Recently Shared on January 25, 2012 at 12:03 pm By:
JMedCaseReports Medical Journal
Latest from #JMCR http://t.co/0W3hFEFj Egyptian baby with ectrodactyly-ectodermal dysplasia-cleft syndrome
Families for HoPE, Inc.
familiesforhope.org — “Families for HoPE, Inc. is a nonprofit organization which provides support to families of infants and children diagnosed with holoprosencephaly, a brain malformation.” View full resource at familiesforhope.org
Most Recently Shared on November 16, 2011 at 8:47 pm By:
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Journal of Medical Case Reports (JMCR) is an open access peer-reviewed journal published by BioMed Central & edited by Prof Michael Kidd.
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