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Results: 1-25/48
Authors:
GELB BD
WILLNER JP
DUNN TM
KARDON NB
VERLOES A
PONCIN J
DESNICK RJ
Citation: Bd. Gelb et al., PATERNAL UNIPARENTAL DISOMY FOR CHROMOSOME-1 REVEALED BY MOLECULAR ANALYSIS OF A PATIENT WITH PYCNODYSOSTOSIS, American journal of human genetics, 62(4), 1998, pp. 848-854
Authors:
VERLOES A
TOUTAIN A
LEMERRER M
Citation: A. Verloes et al., MICROCEPHALIC OSTEODYSPLASTIC DWARFISM TYPE-2, European journal of human genetics, 6, 1998, pp. 104-104
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:
LEROY JG
NUYTINCK L
DEPAEPE A
DERAMMELAERE M
GILLEROT Y
VERLOES A
LOEYS B
DEGROOTE W
Citation: Jg. Leroy et al., BRUCK-SYNDROME - NEONATAL PRESENTATION AND NATURAL COURSE IN 3 PATIENTS, Pediatric radiology, 28(10), 1998, pp. 781-789
Authors:
VANCOSTER RN
JANSSENS S
MISSON JP
VERLOES A
LEROY JG
Citation: Rn. Vancoster et al., PRENATAL-DIAGNOSIS OF PYRUVATE-CARBOXYLASE DEFICIENCY BY DIRECT MEASUREMENT OF CATALYTIC ACTIVITY ON CHORIONIC VILLI SAMPLES, Prenatal diagnosis, 18(10), 1998, pp. 1041-1044
Authors:
ODENT S
LEMAREC B
TOUTAIN A
DAVID A
VIGNERON J
TREGUIER C
JOUAN H
MILON J
FRYNS JP
VERLOES A
Citation: S. Odent et al., CENTRAL-NERVOUS-SYSTEM MALFORMATIONS AND EARLY END-STAGE RENAL-DISEASE IN ORO-FACIO-DIGITAL SYNDROME TYPE-I - A REVIEW, American journal of medical genetics, 75(4), 1998, pp. 389-394
Authors:
PLOMP AS
HAMEL BCJ
COBBEN JM
VERLOES A
OFFERMANS JPM
LAJEUNIE E
FRYNS JP
DEDIESMULDERS CEM
Citation: As. Plomp et al., PFEIFFER SYNDROME TYPE-2 - FURTHER DELINEATION AND REVIEW OF THE LITERATURE, American journal of medical genetics, 75(3), 1998, pp. 245-251
Authors:
VERLOES A
CURRY C
JAMAR M
HERENS C
OLAGUE P
MARKS J
SARDA P
BLANCHET P
Citation: A. Verloes et al., JUVENILE RHEUMATOID-ARTHRITIS AND DEL(22Q11) SYNDROME - A NONRANDOM ASSOCIATION, Journal of Medical Genetics, 35(11), 1998, pp. 943-947
Authors:
LIMET R
NUSGENS B
VERLOES A
SAKALIHASAN N
Citation: R. Limet et al., PATHOGENESIS OF ABDOMINAL AORTIC-ANEURYSM (AAA) FORMATION, Acta Chirurgica Belgica, 98(5), 1998, pp. 195-198
Authors:
GLADWIN A
DONNAI D
METCALFE K
SCHRANDERSTUMPEL C
BRUETON L
VERLOES A
AYLSWORTH A
TORIELLO H
WINTER R
DIXON M
Citation: A. Gladwin et al., LOCALIZATION OF A GENE FOR OCULODENTODIGITAL SYNDROME TO HUMAN-CHROMOSOME 6Q22-Q24, Human molecular genetics, 6(1), 1997, pp. 123-127
Authors:
VERLOES A
LESENFANTS S
Citation: A. Verloes et S. Lesenfants, A NEW FORM OF MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA, Clinical dysmorphology, 6(1), 1997, pp. 21-24
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
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:
COURTENS W
LEVI S
VERBELEN F
VERLOES A
VAMOS E
Citation: W. Courtens et al., FEINGOLD-SYNDROME - REPORT OF A NEW FAMILY AND REVIEW, American journal of medical genetics, 73(1), 1997, pp. 55-60
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
TEMPLE IK
BONNET S
BOTTANI A
Citation: A. Verloes et al., COLOBOMA, MENTAL-RETARDATION, HYPOGONADISM, AND OBESITY - CRITICAL-REVIEW OF THE SO-CALLED BIEMOND SYNDROME TYPE-2, UPDATED NOSOLOGY, AND DELINEATION OF 3 NEW SYNDROMES, American journal of medical genetics, 69(4), 1997, pp. 370-379
Authors:
VERLOES A
LOMBET J
LAMBERT Y
HUBERT AF
DEPREZ M
FRIDMAN V
GOSSEYE S
RIGO J
SOKAL E
Citation: A. Verloes et al., TRICHO-HEPATO-ENTERIC SYNDROME - FURTHER DELINEATION OF A DISTINCT SYNDROME WITH NEONATAL HEMOCHROMATOSIS PHENOTYPE, INTRACTABLE DIARRHEA, AND HAIR ANOMALIES, American journal of medical genetics, 68(4), 1997, pp. 391-395
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
Citation: A. Verloes, OSTEOCRANIOSTENOSIS VS SEVERE HALLERMANN-STREIFF-FRANCOIS SYNDROME, American journal of medical genetics, 68(1), 1997, pp. 105-107
Authors:
VERLOES A
MAQUET P
SADZOT B
VIVARIO M
THIRY A
FRANCK G
Citation: A. Verloes et al., NASU-HAKOLA-SYNDROME - POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY AND PRESENILE-DEMENTIA, Journal of Medical Genetics, 34(9), 1997, pp. 753-757
Authors:
GELB BD
WILLNER JP
VERLOES A
HERENS C
DESNICK RJ
Citation: Bd. Gelb et al., MUTATION ANALYSIS OF PYCNODYSOSTOSIS REVEALS UNIPARENTAL DISOMY OF CHROMOSOME-1, American journal of human genetics, 61(4), 1997, pp. 203-203
Authors:
BIESECKER LG
ABBOTT M
ALLEN J
CLERICUZIO C
FEUILLAN P
GRAHAM JM
HALL T
KANG S
OLNEY AH
LEFTON D
NERI G
PETERS K
VERLOES A
Citation: Lg. Biesecker et al., REPORT FROM THE WORKSHOP ON PALLISTER-HALL SYNDROME AND RELATED PHENOTYPES, American journal of medical genetics, 65(1), 1996, pp. 76-81