DEPIGMENTATION OF HAIR, SKIN AND EYES ASSOCIATED WITH THE APERT SYNDROME
- Author
- MARGOLIS S; SIEGEL IM; CHOY A; BREININ GM
- Source
- BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6B; PP. 341-360; BIBL. 27 REF.
- Document type
- Article
- Language
- English
- Keyword (fr)
- ACROCEPHALOSYNDACTYLIE APERT ALBINISME OCULOCUTANE OEIL ENFANT MALFORMATION CRANE HEREDITAIRE MAIN PIED RACHIS CERVICAL PEAU PATHOLOGIE TROUBLE PIGMENTATION HOMME NEUROLOGIE
- Keyword (en)
- APERT SYNDROME OCULOCUTANEOUS ALBINISM EYE CHILD MALFORMATION SKULLS HEREDITARY HAND FOOT CERVICAL SPINE SKIN DISEASE PIGMENTATION DISORDER HUMAN NEUROLOGY
- Keyword (es)
- NEUROLOGIA
- Classification
- Discipline
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- PASCAL7950372130
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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