Skip to main content
مکتبة رقمیه للعلوم الطبيه
Your cart is empty.
Cart
Lists
Your lists
Log in to create your own lists
Log in to your account
Your cookies
Search history
Search the catalog by:
Library catalog
Title
Author
Subject
ISBN
ISSN
Series
Call number
Search the catalog by keyword
Advanced search
Authority search
Tag cloud
Library
Log in to your account
Home
Advanced search
Results of search for 'au:"Piussan, C"', page 1 of 6
Refine your search
Availability
Limit to records with available items
Authors
Audebert, M
Benhamou, P H
Berquin, P
Boudailliez, B
Canarelli, J P
Colome, M F
Cuvelier, B
Delvallez, N
Denoeux, J P
Epelbaum, S
Frison, B
Goldfarb, A
Grumbach, Y
Krim, G
Lenaerts, C
Mathieu, M
Pautard, J C
Piussan, C
Reguet, C
Risbourg, B
Show more
Show less
Topics
Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Female
Genetic Linkage
Humans
Infant
Infant, Newborn
Intellectual Disability
Male
Pedigree
Syndrome
abnormalities
complications
diagnosis
etiology
genetics
therapeutic use
Show more
Show less
Languages
English
French
Your search returned 117 results.
Sort
1
2
3
4
5
6
Next
Last
Sort by:
Relevance
Popularity (most to least)
Popularity (least to most)
Author (A-Z)
Author (Z-A)
Call number (0-9 to A-Z)
Call number (Z-A to 9-0)
Publication/Copyright date: Newest to oldest
Publication/Copyright date: Oldest to newest
Acquisition date: Newest to oldest
Acquisition date: Oldest to newest
Title (A-Z)
Title (Z-A)
Unhighlight
Highlight
Select all
Clear all
Select titles to:
Add to cart
Add to list
New list
Place hold
Results
1.
[X-linked mental retardation without fragile X chromosome].
[electronic resource]
by
Piussan, C
Producer:
19910509
In:
Archives francaises de pediatrie
vol. 47
Availability:
No items available.
Save to lists
Add to cart
(remove)
2.
[Trisymptomatic disease of Gougerot. (Three cases described in children)].
[electronic resource]
by
Piussan, C
Producer:
19680213
In:
Bulletin de la Societe francaise de dermatologie et de syphiligraphie
vol. 73
Availability:
No items available.
Save to lists
Add to cart
(remove)
3.
[Syndromes of premature aging].
[electronic resource]
by
Piussan, C
Producer:
19930524
In:
Archives francaises de pediatrie
vol. 49
Availability:
No items available.
Save to lists
Add to cart
(remove)
4.
[Werner's syndrome].
[electronic resource]
by
Piussan, C
Producer:
19930201
In:
Archives francaises de pediatrie
vol. 49
Availability:
No items available.
Save to lists
Add to cart
(remove)
5.
[Genetic basis of early aging].
[electronic resource]
by
Piussan, C
Producer:
19930630
In:
Archives francaises de pediatrie
vol. 49
Availability:
No items available.
Save to lists
Add to cart
(remove)
6.
[Teratogenic risk during treatment of Wilson disease].
[electronic resource]
by
Piussan, C
Mathieu, M
Producer:
19851219
In:
Journal de genetique humaine
vol. 33
Availability:
No items available.
Save to lists
Add to cart
(remove)
7.
[Late neurologic evolution of congenital toxoplasmosis demonstrated by study of the cerebrospinal fluid].
[electronic resource]
by
Piussan, C
Desmonts, G
Mozziconacci, P
Producer:
19710907
In:
Pediatrie
vol. 26
Availability:
No items available.
Save to lists
Add to cart
(remove)
8.
[Late neurological development of congenital toxoplasmosis demonstrated by study of the CSF].
[electronic resource]
by
Piussan, C
Desmonts, G
Mozziconacci, P
Producer:
19710608
In:
Annales de pediatrie
vol. 18
Availability:
No items available.
Save to lists
Add to cart
(remove)
9.
[Median dysraphia, chromosomal aberrations and hypopituitarism].
[electronic resource]
by
Boudailliez, B
Piussan, C
Colome, M F
Producer:
19860129
In:
Presse medicale (Paris, France : 1983)
vol. 14
Availability:
No items available.
Save to lists
Add to cart
(remove)
10.
[Gastric acidity. Its correlation with microbial multiplication in the newborn infant's stomach].
[electronic resource]
by
Risbourg, B
Piussan, C
Capron, J P
Producer:
19730724
In:
La Nouvelle presse medicale
vol. 2
Availability:
No items available.
Save to lists
Add to cart
(remove)
11.
[Pancreatitis and pancreactic syndromes in children].
[electronic resource]
by
Malafosse, M
Bienaymé, J
Caille, B
Piussan, C
Producer:
19691105
In:
Annales de pediatrie
vol. 14
Availability:
No items available.
Save to lists
Add to cart
(remove)
12.
[Cerebral and ocular abnormalities with anterior pituitary insufficiency of familial nature].
[electronic resource]
by
Weill, J
Boudailliez, B
Piussan, C
Ponte, C
Producer:
19850514
In:
Journal de genetique humaine
vol. 33
Availability:
No items available.
Save to lists
Add to cart
(remove)
13.
[Bone dysplasia with dwarfism and diffuse skeletal alterations].
[electronic resource]
by
Piussan, C
Maroteaux, P
Castroviejo, I
Risbourg, B
Producer:
19760102
In:
Archives francaises de pediatrie
vol. 32
Availability:
No items available.
Save to lists
Add to cart
(remove)
14.
[Regular dominance of thumb ankylosis with mental retardation transmitted over 3 generations].
[electronic resource]
by
Piussan, C
Lenaerts, C
Mathieu, M
Boudailliez, B
Producer:
19831220
In:
Journal de genetique humaine
vol. 31
Availability:
No items available.
Save to lists
Add to cart
(remove)
15.
Dermatoglyphics in Börjeson-Forssman-Lehmann syndrome.
[electronic resource]
by
Flannery, D B
Piussan, C
Wright, L E
Producer:
19850806
In:
American journal of medical genetics
vol. 21
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
16.
[Waardenburg's syndrome and severe cyanotic cardiopathy].
[electronic resource]
by
Mathieu, M
Bourges, E
Caron, F
Piussan, C
Producer:
19910425
In:
Archives francaises de pediatrie
vol. 47
Availability:
No items available.
Save to lists
Add to cart
(remove)
17.
[Incontinentia pigmenti. Apropos of a case].
[electronic resource]
by
Turut, P
Dumont, P
Piussan, C
Madelain, J
Producer:
19880614
In:
Bulletin des societes d'ophtalmologie de France
vol. 87
Availability:
No items available.
Save to lists
Add to cart
(remove)
18.
[Partial trisomy (10pter leads to 10q21) and partial monosomy (21pter leads to 21q21) due to a reciprocal balanced familial translocation (10;21)(q21;q21) (author's transl)].
[electronic resource]
by
Obry, E
Piussan, C
Risbourg, B
Dutrillaux, B
Producer:
19810613
In:
Annales de genetique
vol. 23
Availability:
No items available.
Save to lists
Add to cart
(remove)
19.
[Megaloblastic anemia due to anticonvulsant therapy].
[electronic resource]
by
Mozziconacci, P
Attai, C
Boisse, J
Piussan, C
Producer:
19691007
In:
Annales de pediatrie
vol. 14
Availability:
No items available.
Save to lists
Add to cart
(remove)
20.
Fragile X mutation and FG syndrome-like phenotype.
[electronic resource]
by
Piussan, C
Mathieu, M
Berquin, P
Fryns, J P
Producer:
19961213
In:
American journal of medical genetics
vol. 64
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)
1
2
3
4
5
6
Next
Last