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Results:
1-9
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Results: 9
Hemifacial microsomia in two patients further supporting chromosomal mosaicism as a causative factor
Authors:
de Ravel, TJL
Legius, E
Brems, H
Van Hoestenberghe, R
Gillis, P
Fryns, JP
Citation: Tjl. De Ravel et al., Hemifacial microsomia in two patients further supporting chromosomal mosaicism as a causative factor, CLIN DYSMOR, 10(4), 2001, pp. 263-267
Authors:
de Ravel, TJL
Matthijs, G
Fryns, JP
Citation: Tjl. De Ravel et al., An unbalanced translocation 46,XX,+der(18)t(18;21)(q12.2;q11.2)mat,-21 associated with maternal isodisomy 18pter -> 18q12.2, ANN GENET, 44(2), 2001, pp. 63-66
Authors:
Manasse, BF
Lekgate, N
Pfaffenzeller, WM
de Ravel, TJL
Citation: Bf. Manasse et al., The Pallister-Killian syndrome is reliably diagnosed by FISH on buccal mucosa, CLIN DYSMOR, 9(3), 2000, pp. 163-165
Authors:
Manasse, BF
Pfaffenzeller, WM
Gurtunca, N
de Ravel, TJL
Citation: Bf. Manasse et al., Brief clinical report - Possible isochromosome 22 leading to trisomy 22, AM J MED G, 95(5), 2000, pp. 411-414
Authors:
Lambie, L
de Ravel, TJL
Citation: L. Lambie et Tjl. De Ravel, Trichorhinophalangeal syndrome type II: Case report, E AFR MED J, 77(1), 2000, pp. 57-59
Authors:
de Ravel, TJL
Berkowitz, DE
Wagner, JM
Jenkins, T
Citation: Tjl. De Ravel et al., Brachydactyly type B with its distinct facies and 'Cooks syndrome' are thesame entity, CLIN DYSMOR, 8(1), 1999, pp. 41-45
Authors:
Viljoen, D
Kromberg, J
de Ravel, TJL
Krause, A
Donaldson, S
Craig, P
Oliveira, V
Citation: D. Viljoen et al., Amniocentesis - Too dangerous and too late?, S AFR MED J, 89(11), 1999, pp. 1118
Authors:
Donaldson, SJF
Wright, CA
de Ravel, TJL
Citation: Sjf. Donaldson et al., Trisomy 18 with total cranio-rachischisis and thoraco-abdominoschisis, PRENAT DIAG, 19(6), 1999, pp. 580-582
Authors:
de Ravel, TJL
van der Griendt, MC
Evan, P
Wright, CA
Citation: Tjl. De Ravel et al., Hydrolethalus syndrome in a non-Finnish family: Confirmation of the entityand early prenatal diagnosis, PRENAT DIAG, 19(3), 1999, pp. 279-281
Risultati:
1-9
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