Renal dysgenesis and KAL1 gene defects in patients with sporadic Kallmann syndrome

Fertility and Sterility

Volumn 88, Issue 5, 2007, Pages 1311-1317

  Georgopoulos, Neoklis A ^a   Koika, Vasiliki ^a   Galli Tsinopoulou, Assimina ^b   Spiliotis, Bessie E ^a   Adonakis, George ^a   Keramida, Maria K ^a   Sgourou, Argyro ^a   Koufogiannis, Kleanthis D ^a   Papachatzopoulou, Adamantia ^a   Papavassiliou, Athanasios G ^a   Kourounis, George ^a   Vagenakis, George A ^a  

^a UNIVERSITY OF PATRAS   (Greece)

^b ARISTOTLE UNIVERSITY OF THESSALONIKI   (Greece)

Author keywords

hypogonadotropic hypogonadism; ichthyosis; KAL1; Kallmann syndrome; renal agenesis; renal dysgenesis

Indexed keywords

ADENINE; ALANINE; GLUTAMIC ACID; GUANINE; LYSINE; STERYL SULFATASE; THREONINE;

ADULT; ARTICLE; CLINICAL ARTICLE; CODON; CORRELATION ANALYSIS; DIAGNOSTIC IMAGING; DNA EXTRACTION; DNA SEQUENCE; ECHOGRAPHY; EXON; GENE; GENE DELETION; GENOTYPE; HUMAN; ICHTHYOSIS; IMAGE ANALYSIS; KAL 1 GENE; KALLMANN SYNDROME; KIDNEY AGENESIS; KIDNEY ANOMALY; KIDNEY STRUCTURE; MALE; NUCLEIC ACID BASE SUBSTITUTION; OUTPATIENT DEPARTMENT; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL; PROSPECTIVE STUDY; SEQUENCE ANALYSIS; SEX LIMITATION; STRUCTURE ANALYSIS; SYNKINESIS; UNIVERSITY HOSPITAL; X CHROMOSOME LINKAGE;

DNA MUTATIONAL ANALYSIS; EXTRACELLULAR MATRIX PROTEINS; HUMANS; KALLMANN SYNDROME; KIDNEY; MALE; MUTATION; NERVE TISSUE PROTEINS; POLYMORPHISM, GENETIC; PROSPECTIVE STUDIES; SEQUENCE DELETION;

EID: 35648970547     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2006.12.044     Document Type: Article

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