Loss of the Y chromosome PAR2 region and additional rearrangements in two familial cases of satellited Y chromosomes: Cytogenetic and molecular analysis

European Journal of Medical Genetics

Volumn 50, Issue 4, 2007, Pages 291-300

  Velissariou, V ^a   Sismani, C ^b   Christopoulou, S ^a   Kaminopetros, P ^a   Hatzaki, A ^a   Evangelidou, P ^b   Koumbaris, G ^b   Bartsocas, C S ^c   Stylianidou, G ^d   Skordis, N ^d   Diakoumakos, A ^a   Patsalis, P C ^b  

^a Mitera Children's Hospital   (Greece)

^b CYPRUS INSTITUTE OF NEUROLOGY AND GENETICS   (Cyprus)

^c Makarios III Hospital Center ^*  (Greece)

^d Makarios III Hospital   (Cyprus)

Author keywords

PAR2 pseudoautosomal region; Y chromosome satellited (Yqs)

Indexed keywords

GROWTH HORMONE; PROLACTIN; SOMATOMEDIN; THYROTROPIN; THYROXINE;

ARTICLE; CASE REPORT; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION; CRANIOFACIAL MALFORMATION; DEVELOPMENTAL DISORDER; FEMALE; GENE LOCUS; GROWTH HORMONE DEFICIENCY; HUMAN; MALE; MOLECULAR BIOLOGY; NEWBORN; OBESITY; PRENATAL DIAGNOSIS; SCHOOL CHILD; Y CHROMOSOME;

ADULT; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, Y; CYTOGENETIC ANALYSIS; DNA, SATELLITE; FAMILY HEALTH; FEMALE; GENE DELETION; GENE REARRANGEMENT; HUMANS; MALE; PHENOTYPE; RECEPTOR, PAR-2; TRANSLOCATION, GENETIC;

EID: 34447318057     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2007.04.004     Document Type: Article

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