Abstract:
:Three families with infants affected with campomelic dysplasia, a genetically determined mesenchymal disease frequently associated with sex reversal were studied. Two XY females with ovarian gonadal differentiation and typical clinical features of campomelic dysplasia could be tested for H-Y antigen and were found to be H-Y negative.
journal_name
Hum Genetjournal_title
Human geneticsauthors
Bricarelli FD,Fraccaro M,Lindsten J,Müller U,Baggio P,Carbone LD,Hjerpe A,Lindgren F,Mayerová A,Ringertz H,Ritzén EM,Rovetta DC,Sicchero C,Wolf Udoi
10.1007/BF00271160subject
Has Abstractpub_date
1981-01-01 00:00:00pages
15-22issue
1eissn
0340-6717issn
1432-1203journal_volume
57pub_type
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