Literature DB >> 11666003

Holoprosencephaly and split hand/foot: an additional case with this rare association.

N Abdel-Meguid, A M Ashour.   

Abstract

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Year:  2001        PMID： 11666003     DOI： 10.1097/00019605-200110000-00008

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN： 0962-8827            Impact factor:   0.816


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  2 in total

Review 1.  Holoprosencephaly and ectrodactyly: Report of three new patients and review of the literature.

Authors:  Amelia A Keaton; Benjamin D Solomon; Anthonie J van Essen; Kathleen M Pfleghaar; Michael A Slama; Judith A Martin; Maximilian Muenke
Journal:  Am J Med Genet C Semin Med Genet       Date:  2010-02-15       Impact factor: 3.908

2.  Novel heterozygous mutation in the extracellular domain of FGFR1 associated with Hartsfield syndrome.

Authors:  Masaki Takagi; Tatsuya Miyoshi; Yuka Nagashima; Nao Shibata; Hiroko Yagi; Ryuji Fukuzawa; Tomonobu Hasegawa
Journal:  Hum Genome Var       Date:  2016-10-13
  2 in total

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