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Results of search for 'au:"STOLL, C"', page 3 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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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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41.
[Complementary therapy in palliative medicine].
[electronic resource]
by
Hübner, J
Stoll, C
Producer:
20110622
In:
Der Internist
vol. 52
Online resources:
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42.
[Trisomy 10 p. Apropos of a case caused by a maternal translocation].
[electronic resource]
by
Stoll, C
Willard, D
Producer:
19800923
In:
Pediatrie
vol. 35
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43.
A boy with neurofibromatosis 1 and Poland anomaly.
[electronic resource]
by
Alembik, Y
Stoll, C
Producer:
19941118
In:
Genetic counseling (Geneva, Switzerland)
vol. 5
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44.
Prenatal diagnosis of dysmorphic syndromes by routine fetal ultrasound examination across Europe.
[electronic resource]
by
Stoll, C
Clementi, M
Producer:
20031209
In:
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
vol. 21
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45.
Long-term follow-up of a girl with oro-facio-digital syndrome type I due to a mutation in the OFD 1 gene.
[electronic resource]
by
Stoll, C
Sauvage, P
Producer:
20030204
In:
Annales de genetique
vol. 45
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46.
The distribution of hypothalamic and extrahypothalamic vasotocinergic cells and fibers in the brain of a lizard, Gekko gecko: presence of a sex difference.
[electronic resource]
by
Stoll, C J
Voorn, P
Producer:
19851113
In:
The Journal of comparative neurology
vol. 239
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47.
[Schooling of children with trisomy 21. A 4-year experience].
[electronic resource]
by
Stoll, C
Roth, M P
Producer:
19830407
In:
Annales de pediatrie
vol. 30
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48.
Segregation of a 22 ring chromosome in three generations.
[electronic resource]
by
Stoll, C
Roth, M P
Producer:
19830729
In:
Human genetics
vol. 63
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49.
[Rheumatoid purpura (Schonlein-Henoch syndrome) in children].
[electronic resource]
by
Levy, J M
Stoll, C
Producer:
19721115
In:
Therapeutique (La Semaine des hopitaux)
vol. 48
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50.
[School attendance of children with trisomy 21. A 4-year experiment].
[electronic resource]
by
Stoll, C
Roth, M P
Producer:
19830826
In:
La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris
vol. 59
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51.
[De novo t(3 ; 20) (p 14 ; p 12) translocation in a young girl].
[electronic resource]
by
Stoll, C
Levy, J M
Producer:
19750509
In:
Annales de genetique
vol. 17
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52.
Identification of a familial Robertsonian translocation t(13q14q) by means of thermic moderated denaturation.
[electronic resource]
by
Stoll, C
Levy, J M
Producer:
19731214
In:
Humangenetik
vol. 19
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53.
[Rheumatoid purpura (Schönlein-Henoch syndrome) in children].
[electronic resource]
by
Lévy, J M
Stoll, C
Producer:
19720210
In:
Annales de pediatrie
vol. 18
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54.
[Familial trisomy 10q (author's transl)].
[electronic resource]
by
Stoll, C
Roth, M P
Producer:
19811216
In:
Archives francaises de pediatrie
vol. 38
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55.
Partial 4q duplication due to inherited der(13),t(4;13)(q26;q34)mat in a girl with a deficiency of factor X.
[electronic resource]
by
Stoll, C
Roth, M P
Producer:
19800712
In:
Human genetics
vol. 53
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56.
[Poland's syndrome in a sterile woman].
[electronic resource]
by
Stoll, C
Schumacher, J C
Producer:
19760311
In:
Journal de genetique humaine
vol. 23
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57.
[Genetic counseling in dermatology].
[electronic resource]
by
Stoll, C
Grosshans, E M
Producer:
19730228
In:
Minerva medica
vol. 63
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58.
Chromosomal region 13q21q31 and heterochrony of development.
[electronic resource]
by
Stoll, C
Martel-Petit, V
Producer:
20060404
In:
Genetic counseling (Geneva, Switzerland)
vol. 16
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59.
Chromosome analysis of spleen and/or lymph nodes of patients with chronic myeloid leukemia (CML).
[electronic resource]
by
Stoll, C
Oberling, F
Flori, E
Producer:
19781129
In:
Blood
vol. 52
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60.
A supraumbilical midline raphé with sternal cleft in a 47,XXX woman.
[electronic resource]
by
Stoll, C
Vivier, M
Renaud, R
Producer:
19870724
In:
American journal of medical genetics
vol. 27
Online resources:
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