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Authors: MEYERS GA DAY D GOLDBERG R DAENTL DL PRZYLEPA KA ABRAMS LJ GRAHAM JM FEINGOLD M RAWNSLEY E SCOTT AF JABS EW
Citation: Ga. Meyers et al., FCFR2 EXON IIIA AND IIIE MUTATIONS IN CROUZON, JACKSON-WEISS, AND PFEIFFER SYNDROMES - EVIDENCE FOR MISSENSE CHANGES, INSERTIONS, AND A DELETION DUE TO ALTERNATIVE RNA SPLICING, American journal of human genetics, 58(3), 1996, pp. 491-498

Authors: MOESCHLER JB FILIANO JJ HANI V RAWNSLEY E
Citation: Jb. Moeschler et al., MOTHER AND DAUGHTER DEMONSTRATING FEATURES OF BOTH ANKYLOBLEPHARON FILIFORME ADNATUM AND CLEFT-PALATE (MIM-NUMBER-106250) AND HAY-WELLS SYNDROME (MIM-NUMBER-106260), American journal of human genetics, 57(4), 1995, pp. 95-95

Authors: ORMOND K GUTTMACHER A KLOZA E DIMAIO M RAWNSLEY E MCGOWAN K WALTERS C
Citation: K. Ormond et al., MATERNAL SERUM SCREENING - THE ATTITUDES AND PRACTICES OF NEW-ENGLANDHEALTH-PROFESSIONALS, American journal of human genetics, 57(4), 1995, pp. 1731-1731

Authors: GAARY EA RAWNSLEY E MARINPADILLA JM MORSE CL CROW HC
Citation: Ea. Gaary et al., INUTERO DETECTION OF FETAL CATARACTS, Journal of ultrasound in medicine, 12(4), 1993, pp. 234-236
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