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Genetic Disorders and the Fetus


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3 3 5 2 2 PCCB Prothrombin deficiency, congenital; F2 F5 AR 2 3 3 3 2 2 Factor V deficiency Pseudovaginal perineoscrotal hypospadias (PPSH) SRD5A2 AR 1 2 2 4 1 1 Rap guanine nucleotide exchange factor 6 (RAPGEF6) RAPGEF6 AD 1 2 3 4 3 1 Renal cell carcinoma, papillary, 1 (RCCP1) MET AD 1 1 2 2 1 1 Renal tubular acidosis, distal, autosomal recessive (RTADR) ATP6V0A4 AR 1 1 2 3 2 1 Renal tubular dysgenesis (RTD) ACE AR 1 4 3 4 2 2 Restrictive dermopathy, lethal ZMPSTE24 AR 2 2 2 3 1 1 Retinal dystrophy, early‐onset, with or without pituitary dysfunction, included OTX2 AD 1 1 0 0 0 0 Retinitis pigmentosa 2 (RP2) RP2 XL 1 1 1 2 1 1 Retinitis pigmentosa 3 (RP3) RPGR XL 5 6 6 8 4 3 Retinitis pigmentosa 4 (RP4) RHO AD 3 5 2 4 1 0 Retinoblastoma (RB1) RB1 AD 17 31 26 43 14 13 Retinoschisis 1, X‐linked, juvenile (RS1) RS1 XL 1 2 1 2 1 0 Rett syndrome (RTT) MECP2 XL 3 5 4 4 3 1 Rhabdoid tumor predisposition syndrome 1 (RTPS1) SMARCB1 AD 1 1 1 1 0 0 Rhesus blood group, D antigen (RHD) RHD AD 7 9 9 16 6 6 Sandhoff disease HEXB AR 4 6 5 8 4 4 Seckel syndrome 1 (SCKL1) ATR AR