Male-to-male transmission in Laurin-Sandrow syndrome and exclusion of RARB and RARG

American Journal of Medical Genetics

Volumn 137 A, Issue 2, 2005, Pages 148-152

  Kjaer, Klaus W ^a,d   Hansen, Lars ^a   Eiberg, Hans ^a   Christensen, Knud Stenild ^b   Opitz, John M ^c   Tommerup, Niels ^a  

^a UNIVERSITY OF COPENHAGEN   (Denmark)

^b AALBORG UNIVERSITY HOSPITAL   (Denmark)

^c UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^d UNIVERSITY OF COPENHAGEN   (Denmark)

Author keywords

Laurin Sandrow syndrome; Mirror image duplication; RARB; RARG

Indexed keywords

RETINOIC ACID RECEPTOR BETA; RETINOIC ACID RECEPTOR GAMMA;

ADULT; ARTICLE; CASE REPORT; CHILD; DNA POLYMORPHISM; EXON; HUMAN; INTRON; LAURIN SANDROW SYNDROME; LIMB DEFECT; MALE; NOSE MALFORMATION; NUCLEIC ACID BASE SUBSTITUTION; PRIORITY JOURNAL; RECEPTOR GENE; SIGNAL TRANSDUCTION; VERTICAL TRANSMISSION;

ABNORMALITIES, MULTIPLE; ADULT; CHILD; FOOT DEFORMITIES, CONGENITAL; GENETIC PREDISPOSITION TO DISEASE; HAND DEFORMITIES, CONGENITAL; HUMANS; INHERITANCE PATTERNS; MALE; NOSE; RECEPTORS, RETINOIC ACID; SEX FACTORS; SYNDROME;

CANIS FAMILIARIS;

EID: 24344510162     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30820     Document Type: Article

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