Couturier-Turpin M H, Ingster O, Salat-Baroux J, Feldmann G
Service d'Histologie, Embryologie, Cytogénétique, Biologie Cellulaire, Hôpital Bichat-Claude Bernard, Paris, France.
Ann Genet. 1994;37(4):200-6.
A new case of familial Yqs is reported. The discovery has been made at the time of karyotyping of a patient with an oligoasthenoteratospermia. A possible correlation between supernumerary NORs of the Yqs chromosome and meiotic disturbances is discussed, and a review of the literature is performed.
