Human PRRX1 and PRRX2 genes: Cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome

Mammalian Genome

Volumn 11, Issue 11, 2000, Pages 1000-1005

  Norris, Russell A ^a   Scott, Karen K ^a   Moore, Clara S ^b   Stetten, Gail ^b   Brown, Cuyler R ^a   Jabs, Ethylin Wang ^b   Wulfsberg, Eric A ^c   Yu, Jack ^d   Kern, Michael J ^a  

^a MEDICAL UNIVERSITY OF SOUTH CAROLINA   (United States)

^b JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF MARYLAND   (United States)

^d MEDICAL COLLEGE OF GEORGIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 1Q; CHROMOSOME 9Q; CLINICAL ARTICLE; CONTROLLED STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION; GENE FUNCTION; GENE LOCATION; GENE MAPPING; GENE MUTATION; HUMAN; HUMAN CELL; HUMAN TISSUE; KIDNEY; LIVER; MOLECULAR CLONING; NAGER ACROFACIAL DYSOSTOSIS; NUCLEOTIDE SEQUENCE; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; STURGE WEBER SYNDROME;

ACRONICTA LEPORINA; GALLUS GALLUS; VERTEBRATA;

EID: 0033769155     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003350010193     Document Type: Article

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