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Results of search for 'au:"STOLL, C"', page 7 of 18
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Authors
Alembik, Y
Baretton, G
Bigel, P
Briegel, J
Clementi, M
De Vigan, C
Dott, B
Feingold, J
Finck, S
Fischbach, M
Grosshans, E
Haller, M
Levy, J M
Lévy, J M
Messer, J
Roth, M P
Schelling, G
Soost, F
Stoll, C
Willard, D
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Topics
Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Chromosome Aberrations
Female
France
Humans
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Infant, Newborn
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Pregnancy
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abnormalities
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121.
[Anomalies in thyroid function in children with trisomy 21].
[electronic resource]
by
Stoll, C
Alembik, Y
Dott, B
Finck, S
Producer:
19900618
In:
Journal de genetique humaine
vol. 37
Availability:
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122.
[Phenotypes of trisomy 13].
[electronic resource]
by
Stoll, C
Willard, D
Demay, M
Weitzenblum, S
Producer:
19731026
In:
Pediatrie
vol. 28
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123.
[A case of trisomy 18 with bilateral aplasia of the radius and thrombopenia].
[electronic resource]
by
Stoll, C
Sacrez, R
Willard, D
Freysz, H
Producer:
19730102
In:
Pediatrie
vol. 27
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124.
[Thymus hypertrophy in the newborn. Effect of lysosome].
[electronic resource]
by
Lévy, J M
Stoll, C
Francfort, J J
Producer:
19710622
In:
Annales de pediatrie
vol. 18
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125.
[Articular contracture with dwarfism and normal intelligence: a new autosomal dominant familial syndrome].
[electronic resource]
by
Stoll, C
Roth, M P
Levy, J M
Producer:
19810421
In:
Journal de genetique humaine
vol. 28
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126.
Different policies on prenatal ultrasound screening programmes and induced abortions explain regional variations in infant mortality with congenital malformations.
[electronic resource]
by
Garne, E
Berghold, A
Johnson, Z
Stoll, C
Producer:
20010712
In:
Fetal diagnosis and therapy
vol. 16
Online resources:
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127.
Radiographic evaluation of the transplant bone height in patients with clefts of the lip/alveolus/palate after secondary bone grafting.
[electronic resource]
by
Opitz, C
Meier, B
Stoll, C
Subklew, D
Producer:
20000119
In:
Journal of orofacial orthopedics = Fortschritte der Kieferorthopadie : Organ/official journal Deutsche Gesellschaft fur Kieferorthopadie
vol. 60
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128.
Refinement of velopharyngoplasty in patients with cleft palate by covering the pharyngeal flap with nasal mucosa from the velum.
[electronic resource]
by
Stoll, C
Hochmuth, M
Meister, P
Soost, F
Producer:
20001012
In:
Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery
vol. 28
Online resources:
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129.
De novo trisomy 22 due to an extra 22Q-chromosome.
[electronic resource]
by
Stoll, C
Medeiros, P
Pécheur, H
Schnebelen, A
Producer:
19980429
In:
Annales de genetique
vol. 40
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130.
No evidence for genomic imprinting in liveborn Down syndrome patients.
[electronic resource]
by
Stoll, C
Alembik, Y
Dott, B
Feingold, J
Producer:
19950830
In:
Annales de genetique
vol. 38
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131.
Lymphedema combined with brachydactyly and tachycardia.
[electronic resource]
by
Stoll, C
Alembik, Y
Dott, B
Kieffer, P
Producer:
19980710
In:
Genetic counseling (Geneva, Switzerland)
vol. 9
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132.
The influence of CD44 splice variants to the outcome of patients with oral squamous cell carcinoma.
[electronic resource]
by
Stoll, C
Baretton, G
Soost, F
Löhrs, U
Producer:
19990318
In:
Advances in experimental medicine and biology
vol. 451
Online resources:
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133.
[Results of active botulinum vaccination].
[electronic resource]
by
FEY, H
STOLL, C
STAHELIN, H
WISEMANN, E
Producer:
19981101
In:
Pathologia et microbiologia
vol. 25
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134.
Familial 13p+ chromosome with mental retardation and dysmorphic features of two children.
[electronic resource]
by
Stoll, C
Rohmer, A
Korn, R
Heumann, G
Producer:
19761201
In:
Human genetics
vol. 34
Online resources:
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135.
Down's syndrome with XYY additional aneuploidy.
[electronic resource]
by
Stoll, C
Frey, D
Willard, D
Messer, J
Producer:
19761201
In:
Human genetics
vol. 34
Online resources:
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136.
Usefulness of chromosome catalog in delineating new syndromes.
[electronic resource]
by
Borgaonkar, D S
Lacassie, Y E
Stoll, C
Producer:
19761101
In:
Birth defects original article series
vol. 12
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137.
[Transitory hypoplastic thrombopenia in trisomy 21. Apropos of 2 cases].
[electronic resource]
by
Stoll, C
Sacrez, R
Willard, D
Freysz, H
Producer:
19720406
In:
Pediatrie
vol. 26
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138.
[Cerebral gigantism. Apropos of a case with a study of somatotropin activity].
[electronic resource]
by
Stoll, C
Luckel, J C
Juif, J G
Producer:
19720406
In:
Pediatrie
vol. 26
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139.
Parental consanguinity as a cause of increased incidence of birth defects in a study of 131,760 consecutive births.
[electronic resource]
by
Stoll, C
Alembik, Y
Dott, B
Feingold, J
Producer:
19940527
In:
American journal of medical genetics
vol. 49
Online resources:
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140.
Evaluation of prenatal diagnosis of cleft lip/palate by foetal ultrasonographic examination.
[electronic resource]
by
Stoll, C
Dott, B
Alembik, Y
Roth, M
Producer:
20000630
In:
Annales de genetique
vol. 43
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