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Results: 1-14 |
Results: 14
THE ENDOSCOPIC APPROACH FOR CONGENITAL NASOLACRIMAL DUCT OBSTRUCTION
Authors: INGELS K KESTELYN P MEIRE F INGELS G VANWEISSENBRUCH R
Citation: K. Ingels et al., THE ENDOSCOPIC APPROACH FOR CONGENITAL NASOLACRIMAL DUCT OBSTRUCTION, Clinical otolaryngology and allied sciences, 22(2), 1997, pp. 96-99
3 NOVEL AND 2 RECURRENT MUTATIONS OF THE NORRIE DISEASE GENE IN PATIENTS WITH NORRIE SYNDROME
Authors: FUCHS S VANDEPOL D BEUDT U KELLNER U MEIRE F BERGER W GAL A
Citation: S. Fuchs et al., 3 NOVEL AND 2 RECURRENT MUTATIONS OF THE NORRIE DISEASE GENE IN PATIENTS WITH NORRIE SYNDROME, Human mutation, 8(1), 1996, pp. 85-88
ARE X-LINKED CONGENITAL STATIONARY NIGET BLINDNESS AND X-LINKED RETINITIS-PIGMENTOSA GENETICALLY ALLELIC
Authors: BERGEN AAB TENBRINK J RIEMSLAG F VANSOEST S SCHUURMAN E MEIRE F TIJMES N DEJONG PTVM
Citation: Aab. Bergen et al., ARE X-LINKED CONGENITAL STATIONARY NIGET BLINDNESS AND X-LINKED RETINITIS-PIGMENTOSA GENETICALLY ALLELIC, Investigative ophthalmology & visual science, 37(3), 1996, pp. 4579-4579
CONCLUSIVE EVIDENCE FOR A DISTINCT CONGENITAL STATIONARY NIGHT BLINDNESS LOCUS IN XP21.1
Authors: BERGEN AAB TENBRINK JB RIEMSLAG F SCHUURMAN EJM MEIRE F TIJMES M DEJONG PTVM
Citation: Aab. Bergen et al., CONCLUSIVE EVIDENCE FOR A DISTINCT CONGENITAL STATIONARY NIGHT BLINDNESS LOCUS IN XP21.1, Journal of Medical Genetics, 33(10), 1996, pp. 869-872
COHEN SYNDROME - THE CLINICAL SYMPTOMS AND STIGMATA AT A YOUNG AGE
Authors: FRYNS JP LEGIUS E DEVRIENDT K MEIRE F STANDAERT L BATEN E VANDENBERGHE H
Citation: Jp. Fryns et al., COHEN SYNDROME - THE CLINICAL SYMPTOMS AND STIGMATA AT A YOUNG AGE, Clinical genetics, 49(5), 1996, pp. 237-241
GENE CONVERSION BETWEEN RED AND DEFECTIVE GREEN OPSIN GENE IN BLUE CONE MONOCHROMACY
Authors: REYNIERS E VANTHIENEN MN MEIRE F BOULLE K DEVRIES K KESTELIJN P WILLEMS PJ
Citation: E. Reyniers et al., GENE CONVERSION BETWEEN RED AND DEFECTIVE GREEN OPSIN GENE IN BLUE CONE MONOCHROMACY, Genomics, 29(2), 1995, pp. 323-328
UNILATERAL CYTOMEGALOVIRUS RETINITIS IN A PATIENT WITH IMMUNOGLOBULING2 DEFICIENCY
Authors: LAFAUT BA VIANNA RNG DEBAETS F MEIRE F
Citation: Ba. Lafaut et al., UNILATERAL CYTOMEGALOVIRUS RETINITIS IN A PATIENT WITH IMMUNOGLOBULING2 DEFICIENCY, Ophthalmologica, 209(1), 1995, pp. 40-43
CHROMOSOME 13Q DELETION WITH WAARDENBURG SYNDROME - FURTHER EVIDENCE FOR A GENE INVOLVED IN NEURAL CREST FUNCTION ON 13Q
Authors: VANCAMP G VANTHIENEN MN HANDIG I VANROY B RAO VS MILUNSKY A READ AP BALDWIN CT FARRER LA BONDUELLE M STANDAERT L MEIRE F WILLEMS PJ
Citation: G. Vancamp et al., CHROMOSOME 13Q DELETION WITH WAARDENBURG SYNDROME - FURTHER EVIDENCE FOR A GENE INVOLVED IN NEURAL CREST FUNCTION ON 13Q, Journal of Medical Genetics, 32(7), 1995, pp. 531-536
LEBER-ASSOCIATED DYSTONIA WITH PUTAMEN NECROSIS
Authors: VANCOSTER R MISSON JP MEIRE F OBERMAIERKUSSER B
Citation: R. Vancoster et al., LEBER-ASSOCIATED DYSTONIA WITH PUTAMEN NECROSIS, Annals of neurology, 36(3), 1994, pp. 522-523
CHROMOSOME-ABERRATIONS IN FIBROUS DYSPLASIA
Authors: DALCIN P SCIOT R SPELEMAN F SAMSON I LAUREYS G DEPOTTER C MEIRE F VANDAMME B VANDENBERGHE H
Citation: P. Dalcin et al., CHROMOSOME-ABERRATIONS IN FIBROUS DYSPLASIA, Cancer genetics and cytogenetics, 77(2), 1994, pp. 114-117
IDENTIFICATION OF A KEY RECOMBINANT WHICH ASSIGNS THE INCOMPLETE CONGENITAL STATIONARY NIGHT BLINDNESS GENE PROXIMAL TO MAOB
Authors: BERGEN AAB KESTELYN P LEYS M MEIRE F
Citation: Aab. Bergen et al., IDENTIFICATION OF A KEY RECOMBINANT WHICH ASSIGNS THE INCOMPLETE CONGENITAL STATIONARY NIGHT BLINDNESS GENE PROXIMAL TO MAOB, Journal of Medical Genetics, 31(7), 1994, pp. 580-582
DNA CARRIER DETECTION IN X-LINKED PROGRESSIVE CONE DYSTROPHY
Authors: BERGEN AAB MEIRE F SCHUURMAN EJM DELLEMAN JW
Citation: Aab. Bergen et al., DNA CARRIER DETECTION IN X-LINKED PROGRESSIVE CONE DYSTROPHY, Clinical genetics, 45(5), 1994, pp. 236-240
FEATURES OF MTDNA MUTATION PATTERNS IN EUROPEAN PEDIGREES AND SPORADIC CASES WITH LEBER HEREDITARY OPTIC NEUROPATHY
Authors: OBERMAIERKUSSER B LORENZ B SCHUBRING S PAPROTTA A ZERRES K MEITINGER T MEIRE F COCHAUX P BLANKENAGEL A KOMMERELL G JAKSCH M GERBITZ KD
Citation: B. Obermaierkusser et al., FEATURES OF MTDNA MUTATION PATTERNS IN EUROPEAN PEDIGREES AND SPORADIC CASES WITH LEBER HEREDITARY OPTIC NEUROPATHY, American journal of human genetics, 55(5), 1994, pp. 1063-1066
ADDITIONAL EVIDENCE FOR A GENE LOCUS FOR PROGRESSIVE CONE DYSTROPHY WITH LATE ROD INVOLVEMENT IN XP21.1-P11.3
Authors: BERGEN AAB MEIRE F TENBRINK J SCHUURMAN EJM VANOMMEN GJB DELLEMAN JW
Citation: Aab. Bergen et al., ADDITIONAL EVIDENCE FOR A GENE LOCUS FOR PROGRESSIVE CONE DYSTROPHY WITH LATE ROD INVOLVEMENT IN XP21.1-P11.3, Genomics, 18(2), 1993, pp. 463-464
Risultati: 1-14 |