Literature DB >> 9605595

Central nervous system anomalies in Seckel syndrome: report of a new family and review of the literature.

A Shanske, R Marion.   

Abstract

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Year:  1998        PMID： 9605595

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  1 in total

1.  Primary Microcephaly with Novel Variant of MCPH1 Gene in Twins: Both Manifesting in Childhood at the Same Time with Hashimoto's Thyroiditis.

Authors:  Piero Pavone; Xena Giada Pappalardo; Andrea Domenico Praticò; Agata Polizzi; Martino Ruggieri; Maria Piccione; Giovanni Corsello; Raffaele Falsaperla
Journal:  J Pediatr Genet       Date:  2020-04-23
  1 in total

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