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Results: 1-6 |
Results: 6

Authors: GEFFROY S EVRARD V TAUFOUR D VANDERBECKEN S DEMARTINVILLE B
Citation: S. Geffroy et al., FURTHER EXAMPLE OF A PATIENT WITH PRADER-WILLI AND KLINEFELTER SYNDROMES OF DIFFERENT PARENTAL ORIGINS, American journal of medical genetics, 80(3), 1998, pp. 286-287

Authors: DEMMER LA KIM JM DEMARTINVILLE B DOWTON SB
Citation: La. Demmer et al., A NOVEL MISSENSE MUTATION IN THE EXON CONTAINING THE PUTATIVE ORNITHINE-BINDING DOMAIN OF THE OTC ENZYME IN A FEMALE, Human mutation, 7(3), 1996, pp. 279-279

Authors: DELAPORTE E JANIN A BLONDEL V COPIN MC PIETTE F DEMARTINVILLE B BERGOEND H
Citation: E. Delaporte et al., LINEAR AND WHORLED NEVOID HYPERMELANOSIS VERSUS INCONTINENTIA PIGMENTI - IS PIGMENTARY INCONTINENCE REALLY A DISTINCTIVE FEATURE, Dermatology, 192(1), 1996, pp. 70-72

Authors: GEFFROY S DEVOS P STAELS B DUBAN B AUWERX J DEMARTINVILLE B
Citation: S. Geffroy et al., LOCALIZATION OF THE HUMAN OB GENE (OBS) TO CHROMOSOME 7Q32 BY FLUORESCENCE IN-SITU HYBRIDIZATION, Genomics, 28(3), 1995, pp. 603-604

Authors: BRACKETT JC SIMS HF STEINER RD NUNGE M ZIMMERMAN EM DEMARTINVILLE B RINALDO P SLAUGH R STRAUSS AW
Citation: Jc. Brackett et al., A NOVEL MUTATION IN MEDIUM-CHAIN ACYL-COA DEHYDROGENASE CAUSES SUDDENNEONATAL DEATH, The Journal of clinical investigation, 94(4), 1994, pp. 1477-1483

Authors: BRACKETT JC SIMS HF MANAHAN CL DEMARTINVILLE B STRAUSS AW
Citation: Jc. Brackett et al., A NOVEL MUTATION IN MEDIUM-CHAIN ACYL-COENZYME-A DEHYDROGENASE CAUSESSUDDEN NEONATAL DEATH, Circulation, 88(4), 1993, pp. 283-283
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