Autosomal recessive Robinow syndrome is allelic to dominant brachydactyly type B and caused by loss of function mutations in ROR2


Afzal A., Rajab A., Fenske C., Oldridge M., Elanko N., Ternes-Pereira E., et al.

JOURNAL OF MEDICAL GENETICS, cilt.37, 2000 (SCI İndekslerine Giren Dergi)

  • Cilt numarası: 37
  • Basım Tarihi: 2000
  • Dergi Adı: JOURNAL OF MEDICAL GENETICS