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The prenatal diagnosis of spinal muscular atrophyMATTHIJS, G; DEVRIENDT, K; FRYNS, J.-P et al.Prenatal diagnosis. 1998, Vol 18, Num 6, pp 607-610, issn 0197-3851Article

Thermal reduction of vanadium pentoxide : an XPD studyDEVRIENDT, K; POELMAN, H; FIERMANS, L et al.Surface science. 1999, Vol 433-35, pp 734-739, issn 0039-6028Article

Deletion in chromosome region 22q11 in a child with CHARGE associationDEVRIENDT, K; SWILLEN, A; FRYNS, J.-P et al.Clinical genetics. 1998, Vol 53, Num 5, pp 408-410, issn 0009-9163Article

Mental retardation, distinct craniofacial dysmorphism, and central nervous system malformation : confirmation of a syndromeDEVRIENDT, K; D'ESPALLIER, L; FRYNS, J.-P et al.Journal of medical genetics. 1996, Vol 33, Num 3, pp 224-226, issn 0022-2593Article

Macrocephaly, hypospadias grade III-IV, and fragile X-like behavior in identical twins without involvement of the FMR-1 geneFRYNS, J. P; D'HOOGHE, M; DEVRIENDT, K et al.Genetic counseling. 1996, Vol 7, Num 3, pp 227-230, issn 1015-8146Article

Progressive extrapyramidal disorder with primary hypogonadism and alopecia in sibs : A new syndrome ?DEVRIENDT, K; LEGIUS, E; FRYNS, J. P et al.American journal of medical genetics. 1996, Vol 62, Num 1, pp 54-57, issn 0148-7299Article

X-ray photoelectron forward scattering and single scattering cluster calculations for V2O5 (001)DEVRIENDT, K; POELMAN, H; FIERMANS, L et al.Solid state communications. 1996, Vol 100, Num 7, pp 481-485, issn 0038-1098Article

Hydrocephalus with features of vaterDEVRIENDT, K; DE COCK, P; FRYNS, J. P et al.Genetic counseling. 1995, Vol 6, Num 1, issn 1015-8146, p. 69Article

Heterochromia of the irides and a motility disorder of the oesophagus: A coincidence or a defect during embryogenesis?GOETHALS, S; HOFFMAN, I; DEVRIENDT, K et al.Bulletin de la Société belge d'ophtalmologie. 2003, Num 289, pp 73-77, issn 0081-0746, 5 p.Article

The V2O5/TiO2 (anatase) model catalyst structure : XPD study and single scattering cluster simulationsDEVRIENDT, K; POELMAN, H; FIERMANS, L et al.Surface and interface analysis. 2000, Vol 29, Num 2, pp 139-144, issn 0142-2421Article

A 3p deletion syndrome in a child with both del(3)(p25→pter) and dup(17)(q23→qter)LUKUSA, T; DEVRIENDT, K; FRYNS, J. P et al.Annales de génétique (Paris). 1999, Vol 42, Num 2, pp 91-94, issn 0003-3995Article

Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD)DEBEER, Ph; VAN ESCH, H; HUYSMANS, C et al.European journal of medical genetics. 2005, Vol 48, Num 4, pp 377-387, issn 1769-7212, 11 p.Article

Work function engineering by FUSI and its impact on the performance and reliability of oxynitride and Hf-silicate based MOSFETsVELOSO, A; ANIL, K. G; JURCZAK, M et al.International Electron Devices Meeting. 2004, pp 855-858, isbn 0-7803-8684-1, 1Vol, 4 p.Conference Paper

PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mousePEETERS, H; DEBEER, P; VAN DE VEN, W et al.Human genetics. 2003, Vol 112, Num 5-6, pp 573-580, issn 0340-6717, 8 p.Article

Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH)WITTERS, Ingrid; DEVRIENDT, K; LEGIUS, E et al.Prenatal diagnosis. 2002, Vol 22, Num 1, pp 29-33, issn 0197-3851Article

Two siblings with early onset fetal akinesia deformation sequence and hydranencephaly: Further evidence for autosomal recessive inheritance of hydranencephaly, Fowler typeWITTERS, I; MOERMAN, Ph; DEVRIENDT, K et al.American journal of medical genetics. 2002, Vol 108, Num 1, pp 41-44, issn 0148-7299Article

Bilateral tibial agenesis with ectrodactyly (OMIM 119100): Further evidence for autosomal recessive inheritanceWITTERS, I; DEVRIENDT, K; MOERMAN, Ph et al.American journal of medical genetics. 2001, Vol 104, Num 3, pp 209-213, issn 0148-7299Article

Deletion of NKX2.1 gene encoding thyroid transcription factor-1 in two siblings with hypothyroidism and respiratory failureIWATANI, N; MABE, H; DEVRIENDT, K et al.The Journal of pediatrics. 2000, Vol 137, Num 2, pp 272-276, issn 0022-3476Article

Novel syndromic form of X-linked complicated spastic paraplegiaCLAES, S; DEVRIENDT, K; VAN GOETHEM, G et al.American journal of medical genetics. 2000, Vol 94, Num 1, pp 1-4, issn 0148-7299Article

Partial DiGeorge syndrome in two patients with a 10p rearrangementVAN ESCH, H; GROENEN, P; DAW, S et al.Clinical genetics. 1999, Vol 55, Num 4, pp 269-276, issn 0009-9163Article

A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8CLAEYS, I; HOLVOET, M; EYSKENS, B et al.American journal of medical genetics. 1997, Vol 74, Num 5, pp 515-520, issn 0148-7299Article

Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndromeDEVRIENDT, K; PETIT, P; MATTHIJS, G et al.Journal of medical genetics. 1997, Vol 34, Num 5, pp 395-399, issn 0022-2593Article

Paucity of intrahepatic bile ducts, solitary kidney and atrophic pancreas with diabetes mellitus : atypical Alagille syndrome ?DEVRIENDT, K; DOOMS, L; PROESMANS, W et al.European journal of pediatrics. 1996, Vol 155, Num 2, pp 87-90, issn 0340-6199Conference Paper

Diaphragmatic hernia in Denys-Drash syndromeDEVRIENDT, K; DELOOF, E; MOERMAN, P et al.American journal of medical genetics. 1995, Vol 57, Num 1, pp 97-101, issn 0148-7299Article

Recurrent reciprocal deletions and duplications of 16p13.11 : the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variantHANNES, F. D; SHARP, A. J; STEWART, H et al.Journal of medical genetics. 2009, Vol 46, Num 4, pp 223-232, issn 0022-2593, 10 p.Article

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