The mouse Mid1 gene: Implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region

Human Molecular Genetics

Volumn 7, Issue 3, 1998, Pages 489-499

  Dal Zotto, Laura ^a   Quaderi, Nandita A ^a   Elliott, Rosemary ^b   Lingerfelter, Patricia A ^c   Carrel, Laura ^d   Valsecchi, Valentina ^a   Montini, Eugenio ^a   Yen, Chao Huang ^b,g   Chapman, Verne ^b   Kalcheva, Iveta ^b,h   Arrigo, Giulia ^e,f   Zuffardi, Orsetta ^e,f   Thomas, Sushma ^c   Willard, Huntington F ^d   Ballabio, Andrea ^a   Disteche, Christine M ^c   Rugarli, Elena I ^a  

^a TELETHON INSTITUTE OF GENETICS AND MEDICINE TIGEM   (Italy)

^b ROSWELL PARK CANCER INSTITUTE   (United States)

^c UNIVERSITY OF WASHINGTON   (United States)

^d CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e Servizio di Citogenetica   (Italy)

^f UNIVERSITY OF PAVIA   (Italy)

^g SAIC FREDERICK INC   (United States)

^h Gene/Networks Inc   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ZINC FINGER PROTEIN;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CENTRAL NERVOUS SYSTEM; CROSSING OVER; DEVELOPMENTAL GENETICS; EVOLUTION; FLUORESCENCE IN SITU HYBRIDIZATION; GASTROINTESTINAL TRACT; GENE; GENE DELETION; GENE DUPLICATION; GENE EXPRESSION; GENE LOCATION; GENETIC STABILITY; MALE; MALFORMATION SYNDROME; MOLECULAR CLONING; MOUSE; NONHUMAN; OPITZ SYNDROME; PATHOGENESIS; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; SPECIES DIFFERENCE; TISSUE DISTRIBUTION; UROGENITAL SYSTEM; X CHROMOSOME;

ABNORMALITIES, MULTIPLE; ANIMALS; CHROMOSOME MAPPING; CROSSES, GENETIC; EMBRYONIC AND FETAL DEVELOPMENT; EVOLUTION; FEMALE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HUMANS; MALE; MAMMALS; MICE; MICE, INBRED C57BL; MICROTUBULE PROTEINS; MOLECULAR SEQUENCE DATA; NUCLEAR PROTEINS; PSEUDOGENES; TRANSCRIPTION FACTORS; X CHROMOSOME; ZINC FINGERS;

EID: 6844261193     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/7.3.489     Document Type: Article

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