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Results: 1-7 |
Results: 7

Authors: KNOLL KHM REPETTO G DERKALOUSTIAN V MUNDLOS C EYDOUX P KORF B WHITE LM
Citation: Khm. Knoll et al., LARGE DICENTRIC CHROMOSOME 15Q11Q13 DUPLICATIONS - MULTIPLE REGIONS OF BREAKAGE, MECHANISMS OF FORMATION AND CLINICAL FINDINGS, American journal of human genetics, 61(4), 1997, pp. 23-23

Authors: GERBER S LARGETPIET D ROZET JM BONNEAU D MATHIEU M DERKALOUSTIAN V MUNNICH A KAPLAN J
Citation: S. Gerber et al., EVIDENCE FOR A FOURTH LOCUS IN USHER SYNDROME TYPE-I, Journal of Medical Genetics, 33(1), 1996, pp. 77-79

Authors: LARGETPIET D GERBER S ROZET JM BONNEAU D MATHIEU M DERKALOUSTIAN V MUNNICH A KAPLAN J
Citation: D. Largetpiet et al., EVIDENCE FOR A 4TH LOCUS RESPONSIBLE FOR USHER SYNDROME TYPE-I (USID), Vision research, 35, 1995, pp. 3234-3234

Authors: WHITE LM DERKALOUSTIAN V NAEEM R KNOLL JHM
Citation: Lm. White et al., CHROMOSOME 15Q11Q13 DUPLICATIONS - MECHANISM OF FORMATION, American journal of human genetics, 57(4), 1995, pp. 731-731

Authors: LARGETPIET D GERBER S ROZET JM BONNEAU D MATHIEU M DERKALOUSTIAN V MUNNICH A KAPLAN J
Citation: D. Largetpiet et al., EVIDENCE FOR A 4TH LOCUS RESPONSIBLE FOR USHER-SYNDROME TYPE-I (USID), American journal of human genetics, 57(4), 1995, pp. 1885-1885

Authors: ROUSSEAU F ROBB L DERKALOUSTIAN V
Citation: F. Rousseau et al., A MENTALLY NORMAL-MALE CARRIER OF A FRAGILE-X FULL MUTATION GAVE BIRTH TO A PREMUTATED DAUGHTER, American journal of human genetics, 53(3), 1993, pp. 1222-1222

Authors: PRATT VM BOYADJEV S DLOUHY S SILVER K DERKALOUSTIAN V HODES ME
Citation: Vm. Pratt et al., PELIZAEUS-MERZBACHER DISEASE IN A FAMILY OF PORTUGUESE ORIGIN CAUSED BY A POINT MUTATION IN EXON 5 OF THE PLP GENE, American journal of human genetics, 53(3), 1993, pp. 1751-1751
Risultati: 1-7 |