Mendelian puzzles

Science

Volumn 335, Issue 6071, 2012, Pages 930-931

  Chakravarti, Aravinda ^a   Kapoor, Ashish ^a  

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

Author keywords

[No Author keywords available]

Indexed keywords

DEVELOPMENTAL BIOLOGY; ENZYME ACTIVITY; GENE EXPRESSION; GENETIC ANALYSIS; MUTATION; PHENOTYPE; PROTEIN;

CHROMOSOME; GENE MUTATION; GENETIC DISORDER; GENETIC POLYMORPHISM; GENETICS; GENOME; HEART INFARCTION; HIRSCHSPRUNG DISEASE; HUMAN; HUMAN GENOME; JOUBERT SYNDROME; PHENOTYPE; PHENYLKETONURIA; PRIORITY JOURNAL; SHORT SURVEY; ANIMAL; CEREBELLUM DISEASE; CONGENITAL MALFORMATION; EUKARYOTIC FLAGELLUM; EYE MALFORMATION; GENE EXPRESSION REGULATION; GENE LOCUS; KIDNEY POLYCYSTIC DISEASE; MOLECULAR EVOLUTION; NOTE; REGULATORY SEQUENCE; RETINA; ULTRASTRUCTURE;

MEMBRANE PROTEIN; TMEM138 PROTEIN, HUMAN; TMEM216 PROTEIN, HUMAN;

ANIMALS; CEREBELLAR DISEASES; CILIA; EVOLUTION, MOLECULAR; EYE ABNORMALITIES; GENE EXPRESSION REGULATION; GENETIC LOCI; HUMANS; KIDNEY DISEASES, CYSTIC; MEMBRANE PROTEINS; REGULATORY SEQUENCES, NUCLEIC ACID; RETINA;

EID: 84857562364     PISSN: 00368075     EISSN: 10959203     Source Type: Journal    
DOI: 10.1126/science.1219301     Document Type: Short Survey

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