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1-24
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Results: 24
Authors:
KOULISCHER L
GILLEROT Y
HERENS C
JAMAR M
VERLOES A
FOURNEAU C
Citation: L. Koulischer et al., TRIPLE TEST AND NEW INCIDENCE OF TRISOMY-21 AT BIRTH IN SOUTH BELGIUM, European journal of human genetics, 6, 1998, pp. 1141-1141
Authors:
HERENS C
THIRY JC
JAMAR M
SCHOOS R
VERLOES A
KOULISCHER L
Citation: C. Herens et al., CRI DU CHAT ASSOCIATED WITH A COMPLEX REARRANGEMENT IN THE SON OF A WOMAN WITH A T(4 17) BALANCED TRANSLOCATION/, European journal of human genetics, 6, 1998, pp. 2090-2090
Authors:
JAMAR M
HERENS C
PONCIN J
LESENFANTS S
KOULISCHER L
Citation: M. Jamar et al., SOCIAL OUTCOME OF UNEXPECTED CHROMOSOMAL-ABNORMALITIES, European journal of human genetics, 6, 1998, pp. 6038-6038
Authors:
THIRY JC
JAMAR M
KOULISCHER L
HERENS C
Citation: Jc. Thiry et al., PREDICTIVENESS AND SENSITIVITY OF FISH DATA FOR THE FOLLOW-UPS OF OPPOSITE-SEX BONE-MARROW TRANSPLANTATION PATIENTS USING CENTROMERIC PROBES FOR CHROMOSOME-X AND CHROMOSOME-Y, Cytogenetics and cell genetics, 81(2), 1998, pp. 198-198
Authors:
KOULISCHER L
Citation: L. Koulischer, TEACHING AND PRECONDITIONS OF PROFESSIONAL PRACTICE IN CYTOGENETICS -ETHICAL ASPECTS, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 62-62
Authors:
ASLANIS P
JAMAR M
HERENS C
KOULISCHER L
Citation: P. Aslanis et al., MEIOTIC CHROMOSOME-STUDIES IN A SAMPLE OF STERILE MALE-PATIENTS, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 108-108
Authors:
SCHOOS R
SGOURAS D
LESENFANT S
VERLOES A
JAMAR H
HERENS C
GIRGINOUDIS P
PANGALOS C
KOULISCHER L
Citation: R. Schoos et al., TRISOMY-21 RISK-EVALUATION AT THE FIRST-TRIMESTER OF GESTATION BY ELISA FOR PAPP-ALPHA, FREE-BETA-HCG AND UNCONJUGATED ESTRIOL IN DRY BLOOD-SAMPLES - A PROSPECTIVE-STUDY ON 805 PATIENTS, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 185-185
Authors:
SCHOOS R
VERLOES A
LESENFANT S
JAMAR M
HERENS C
KOULISCHER L
Citation: R. Schoos et al., TRISOMY-21 RISK-EVALUATION AT 2ND-TRIMESTER OF GESTATION BY ELISA, FOR AFP, HCG AND UE3 ON DRIED BLOOD-SAMPLES - A MASS-SCREENING ON 46,000WOMEN, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 186-186
Authors:
JAMAR M
VERLOES A
HERENS C
TRUILLET M
LHOMME A
KOULISCHER L
Citation: M. Jamar et al., STUDY OF A FAMILIAL TRANSLOCATION T(10-13), Cytogenetics and cell genetics, 77(1-2), 1997, pp. 234-234
Authors:
HERENS C
HERMANNE JP
TASSIN F
FASSOTTE MF
JAMAR M
SCHAAFLAFONTAINE N
FILLET G
KOULISCHER L
Citation: C. Herens et al., T(2-3)(P23-Q27) AS THE SOLE ANOMALY IN A CASE OF MYELOFIBROSIS, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 317-317
Authors:
HERENS C
JAMAR M
ALVAREZGONZALEZ ML
LESENFANTS S
LOMBET J
BONNIVERT J
KOULISCHER L
VERLOES A
Citation: C. Herens et al., PRIVATE MULTIPLE CONGENITAL ANOMALY SYNDROMES MAY RESULT FROM UNBALANCED SUBTLE TRANSLOCATIONS - T(2Q-4P) EXPLAINS THE LAMBOTTE-SYNDROME, American journal of medical genetics, 73(2), 1997, pp. 127-131
Authors:
VERLOES A
MASSIN M
LOMBET J
GRATTAGLIANO B
SOYEUR D
RIGO J
KOULISCHER L
VANHOOF F
Citation: A. Verloes et al., NOSOLOGY OF LYSOSOMAL GLYCOGEN-STORAGE DISEASES WITHOUT IN-VITRO ACIDMALTASE DEFICIENCY - DELINEATION OF A NEONATAL FORM, American journal of medical genetics, 72(2), 1997, pp. 135-142
Authors:
VERLOES A
LESENFANTS S
MISSON JP
GALAND A
KOULISCHER L
Citation: A. Verloes et al., MICROCEPHALY, MUSCULAR BUILD, RHIZOMELIA, AND CATARACTS - DESCRIPTIONOF A POSSIBLE RECESSIVE SYNDROME AND SOME COMMENTS ON THE USE OF ELECTRONIC DATABASES IN SYNDROMOLOGY, American journal of medical genetics, 68(4), 1997, pp. 455-460
Authors:
VERLOES A
TEMPLE IK
HUBERT AF
HOPE P
GOULD S
DEBAUCHE C
VERELLEN G
DEVILLE JL
KOULISCHER L
SOKAL EM
Citation: A. Verloes et al., RECURRENCE OF NEONATAL HEMOCHROMATOSIS IN HALF SIBS BORN OF UNAFFECTED MOTHERS, Journal of Medical Genetics, 33(6), 1996, pp. 444-449
Authors:
VERLOES A
JAMBLIN P
KOULISCHER L
BOURGUIGNON JP
Citation: A. Verloes et al., A NEW FORM OF SKELETAL DYSPLASIA WITH AMELOGENESIS IMPERFECTA AND PLATYSPONDYLY, Clinical genetics, 49(1), 1996, pp. 2-5
Authors:
VERLOES A
SAKALIHASAN N
KOULISCHER L
LIMET R
Citation: A. Verloes et al., ANEURYSMS OF THE ABDOMINAL-AORTA - FAMILIAL AND GENETIC-ASPECTS IN 313 PEDIGREES, Journal of vascular surgery, 21(4), 1995, pp. 646-655
Authors:
ECTORS FJ
KOULISCHER L
JAMAR M
HERENS C
VERLOES A
REMY B
BECKERS JF
Citation: Fj. Ectors et al., CYTOGENETIC STUDY OF BOVINE OOCYTES MATURED IN-VITRO, Theriogenology, 44(3), 1995, pp. 445-450
Authors:
HERENS C
JACQUEMART M
KOULISCHER L
BARBASON H
Citation: C. Herens et al., NUCLEAR LESIONS DURING RAT HEPATOCARCINOGENESIS .1. MEASURING THE SISTER-CHROMATID EXCHANGES DURING INITIATION, PROMOTION AND PROGRESSION OF RAT HEPATOCARCINOGENESIS INDUCED WITH DIETHYLNITROSAMINE, Mutation research, 329(2), 1995, pp. 153-159
Authors:
HERENS C
MASSART S
BOUZAHZAH B
KOULISCHER L
BARBASON H
Citation: C. Herens et al., NUCLEAR LESIONS DURING RAT HEPATOCARCINOGENESIS .2. MEASURING THE MICRONUCLEI DURING INITIATION, PROMOTION AND PROGRESSION OF RAT HEPATOCARCINOGENESIS INDUCED WITH DIETHYLNITROSAMINE, Mutation research, 329(2), 1995, pp. 161-171
Authors:
VERLOES A
MASSART B
DEHALLEUX I
LANGHENDRIES JP
KOULISCHER L
Citation: A. Verloes et al., CLINICAL OVERLAP OF BECKWITH-WIEDEMANN, PERLMAN AND SIMPSON-GOLABI-BEHMEL SYNDROMES - A DIAGNOSTIC PITFALL, Clinical genetics, 47(5), 1995, pp. 257-262
Authors:
VERLOES A
SCHOOS R
HERENS C
VINTENS A
KOULISCHER L
Citation: A. Verloes et al., A PRENATAL TRISOMY-21 SCREENING-PROGRAM USING ALPHA-FETOPROTEIN, HUMAN CHORIONIC-GONADOTROPIN, AND FREE ESTRIOL ASSAYS ON MATERNAL DRIED BLOOD, American journal of obstetrics and gynecology, 172(1), 1995, pp. 167-174
Authors:
ALBERING HJ
ENGELEN JJ
KOULISCHER L
WELLE IJ
KLEINJANS JC
Citation: Hj. Albering et al., INDOOR RADON, AN EXTRAPULMONARY GENETIC RISK, Lancet, 344(8924), 1994, pp. 750-751
Authors:
HUSTINX R
VERLOES A
GRATTAGLIANO B
HERENS C
JAMAR M
SOYEUR D
SCHAAPS JP
KOULISCHER L
Citation: R. Hustinx et al., MONOSOMY-11Q - REPORT OF 2 FAMILIAL CASES AND REVIEW OF THE LITERATURE, American journal of medical genetics, 47(3), 1993, pp. 312-317
Authors:
VERLOES A
BRICTEUX G
KOULISCHER L
Citation: A. Verloes et al., PSEUDOAMINOPTERIN SYNDROME, American journal of medical genetics, 46(4), 1993, pp. 394-397
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1-24
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