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Results of search for 'au:"De Ravel, T"', page 1 of 3
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Authors
Altay, C
Balikova, I
Brunner, H G
Chabchoub, E
Cohn, R J
Davies, V A
De Ravel, T J
Devriendt, K
Dokal, I
Fryns, J P
Fryns, J-P
Gibson, R A
Havenga, C
Jansen, S
Matthijs, G
Thienpont, B
Vermeesch, J R
de Ravel, T
de Ravel, T J
de Ravel, T J L
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Topics
Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Chromosome Aberrations
Female
Humans
In Situ Hybridization, Fluorescence
Infant
Infant, Newborn
Intellectual Disability
Male
Middle Aged
Mutation
Phenotype
Pregnancy
Syndrome
abnormalities
genetics
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English
French
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1.
Trichorhinophalangeal syndrome type II: case report.
[electronic resource]
by
Lambie, L
de Ravel, T J
Producer:
20000831
In:
East African medical journal
vol. 77
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2.
An unbalanced translocation 46,XX,+der(18)t(18;21)(q12.2;q11.2)mat,-21 associated with maternal isodisomy 18pter-->18q12.2.
[electronic resource]
by
de Ravel, T J
Matthijs, G
Fryns, J
Producer:
20011204
In:
Annales de genetique
vol. 44
Online resources:
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3.
The obstetrician's dilemma during delivery of the very-low-birth-weight infant.
[electronic resource]
by
van der Griendt, M C
de Ravel, T
Guidozzi, F
Producer:
19920508
In:
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde
vol. 81
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4.
Trisomy 18 with total cranio-rachischisis and thoraco-abdominoschisis.
[electronic resource]
by
Donaldson, S J
Wright, C A
de Ravel, T J
Producer:
19991202
In:
Prenatal diagnosis
vol. 19
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5.
"A new association of mental retardation, short stature, unusual face, radio-ulnar synostosis and retinal pigment abnormalities": Cohen syndrome with thrombocytopenia.
[electronic resource]
by
De Ravel, T J L
Dillen, K
Fryns, J P
Producer:
20030425
In:
Genetic counseling (Geneva, Switzerland)
vol. 13
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6.
Cohen syndrome and rheumatoid arthritis.
[electronic resource]
by
De Ravel, T J L
Azou, M
Fryns, J R
Producer:
20021129
In:
Genetic counseling (Geneva, Switzerland)
vol. 13
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7.
Postmortem findings in three triploid fetuses.
[electronic resource]
by
de Ravel, T J
Wright, C A
Moller, L I
Producer:
19970421
In:
Birth defects original article series
vol. 30
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8.
Tetra-amelia and splenogonadal fusion in Roberts syndrome.
[electronic resource]
by
de Ravel, T J
Seftel, M D
Wright, C A
Producer:
19970425
In:
American journal of medical genetics
vol. 68
Online resources:
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9.
Trisomy 8 mosaicism: a further five cases illustrating marked clinical and cytogenetic variability.
[electronic resource]
by
Jordan, M A
Marques, I
Rosendorff, J
de Ravel, T J
Producer:
19980922
In:
Genetic counseling (Geneva, Switzerland)
vol. 9
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10.
De novo interstitial tandem duplication of chromosome 20p12.1p13.
[electronic resource]
by
de Ravel, T J L
Vermeesch, J R
Fryns, J-P
Producer:
20030520
In:
American journal of medical genetics. Part A
vol. 117A
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11.
Apparently new autosomal dominant Spondyloepimetaphyseal dysplasia: gonadal mosaicism onset.
[electronic resource]
by
de Ravel, T J L
De Smet, L
Fryns, J-P
Producer:
20030312
In:
Clinical dysmorphology
vol. 11
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12.
Macrocephaly, mental retardation, dysmorphism, and spastic paraplegia.
[electronic resource]
by
de Ravel, T J L
Van Driessche, J
Fryns, J P
Producer:
20050222
In:
American journal of medical genetics. Part A
vol. 127A
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13.
Pulmonary arterio-venous malformations in a patient with a novel mutation in exon 10 of the ACVRL1 gene.
[electronic resource]
by
Vandenbriele, C
Peerlinck, K
de Ravel, T
Verhamme, P
Vanassche, T
Producer:
20140617
In:
Acta clinica Belgica
vol. 69
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14.
Possible isochromosome 22 leading to trisomy 22.
[electronic resource]
by
Manasse, B F
Pfaffenzeller, W M
Gurtunca, N
de Ravel, T J
Producer:
20010125
In:
American journal of medical genetics
vol. 95
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15.
Brachydactyly type B with its distinct facies and 'Cooks syndrome' are the same entity.
[electronic resource]
by
de Ravel, T J
Berkowitz, D E
Wagner, J M
Jenkins, T
Producer:
19990628
In:
Clinical dysmorphology
vol. 8
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16.
The Pallister-Killian syndrome is reliably diagnosed by FISH on buccal mucosa.
[electronic resource]
by
Manasse, B F
Lekgate, N
Pfaffenzeller, W M
de Ravel, T J
Producer:
20001207
In:
Clinical dysmorphology
vol. 9
Online resources:
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17.
Lethal neonatal mandibuloacral dysplasia.
[electronic resource]
by
Seftel, M D
Wright, C A
Po, P L
de Ravel, T J
Producer:
19970312
In:
American journal of medical genetics
vol. 66
Online resources:
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18.
Chimerism in black southern African patients with true hermaphroditism 46,XX/47XY,+21 and 46,XX/46,XY.
[electronic resource]
by
Ramsay, M
Pfaffenzeller, W
Kotze, E
Bhengu, L
Essop, F
de Ravel, T
Producer:
20090210
In:
Annals of the New York Academy of Sciences
vol. 1151
Online resources:
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19.
The ICF syndrome: new case and update.
[electronic resource]
by
De Ravel, T J
Deckers, E
Alliet, P L
Petit, P
Fryns, J P
Producer:
20020723
In:
Genetic counseling (Geneva, Switzerland)
vol. 12
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20.
Complex chromosome re-arrangement 45,X,t(Y;9) in a girl with sex reversal and mental retardation.
[electronic resource]
by
de Ravel, T J L
Fryns, J P
Van Driessche, J
Vermeesch, J R
Producer:
20040728
In:
American journal of medical genetics. Part A
vol. 124A
Online resources:
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