Genetic disorders of pigmentation

Advances in Human Genetics

Volumn 22, Issue , 1994, Pages 1-45

  Spritz, R A ^a   Hearing Jr , V J ^a  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MELANIN; MONOPHENOL MONOOXYGENASE;

CHROMOSOMAL LOCALIZATION; GENE LOCATION; GENE LOCUS; HUMAN; MELANOCYTE; MELANOGENESIS; MICROPHTHALMIA; MOLECULAR CLONING; MOUSE; MUTATION RATE; NONHUMAN; NUCLEIC ACID BASE SUBSTITUTION; OCULOCUTANEOUS ALBINISM; PIEBALDISM; PIGMENT DISORDER; PRIORITY JOURNAL; REVIEW; WAARDENBURG SYNDROME;

EID: 0028610286     PISSN: 0065275X     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-4757-9062-7_1     Document Type: Review

References (0)