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European Journal of Pediatrics
|
February 1, 1988
The acrocallosal syndrome
N Philip, N Apicella, I Lassman, et al.
American Journal of Medical Genetics
|
November 4, 1998
Microcephalic osteodysplastic primordial dwarfism Taybi-Linder type: report of four cases and review of the literature
S Sigaudy, A Toutain, A Moncla, et al.
Journal of Mental Deficiency Research
|
September 1, 1979
Erythrocyte copper levels in children with trisomy 21
B Mallet, P Poulet, S Ayme, et al.
Revue De Chirurgie Orthopedique Et Reparatrice De L'Appareil Moteur
|
January 1, 1988
[Congenital scoliosis in homozygote twins. Apropos of a case report]
M Bergoin, F Giraud, N Philipp, et al.
Prenatal Diagnosis
|
May 1, 1990
Socio-cultural inequities in access to prenatal diagnosis: the role of insurance coverage and regulatory policies
J P Moatti, C Le Gales, C Julian, et al.
Annales De Genetique
|
January 1, 1995
Distribution of single organ malformations in European populations. EUROCAT Working Group
C Stoll, S Ayme, R Beckers, et al.
Clinical Dysmorphology
|
April 1, 1992
Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 16 non-Japanese cases
N Philip, P Meinecke, A David, et al.
Teratology
|
November 1, 1991
Heterogeneity of neural tube defects in Europe: the significance of site of defect and presence of other major anomalies in relation to geographic differences in prevalence
H Dolk, P De Wals, Y Gillerot, et al.
Journal De Genetique Humaine
|
September 1, 1981
[Consanguineous marriages in genetic consultation]
M L Briard, J Kaplan, S Ayme, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 49 results.
European Journal of Pediatrics
|
February 1, 1988
The acrocallosal syndrome
N Philip, N Apicella, I Lassman, et al.
American Journal of Medical Genetics
|
November 4, 1998
Microcephalic osteodysplastic primordial dwarfism Taybi-Linder type: report of four cases and review of the literature
S Sigaudy, A Toutain, A Moncla, et al.
Journal of Mental Deficiency Research
|
September 1, 1979
Erythrocyte copper levels in children with trisomy 21
B Mallet, P Poulet, S Ayme, et al.
Revue De Chirurgie Orthopedique Et Reparatrice De L'Appareil Moteur
|
January 1, 1988
[Congenital scoliosis in homozygote twins. Apropos of a case report]
M Bergoin, F Giraud, N Philipp, et al.
Prenatal Diagnosis
|
May 1, 1990
Socio-cultural inequities in access to prenatal diagnosis: the role of insurance coverage and regulatory policies
J P Moatti, C Le Gales, C Julian, et al.
Annales De Genetique
|
January 1, 1995
Distribution of single organ malformations in European populations. EUROCAT Working Group
C Stoll, S Ayme, R Beckers, et al.
Clinical Dysmorphology
|
April 1, 1992
Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 16 non-Japanese cases
N Philip, P Meinecke, A David, et al.
Teratology
|
November 1, 1991
Heterogeneity of neural tube defects in Europe: the significance of site of defect and presence of other major anomalies in relation to geographic differences in prevalence
H Dolk, P De Wals, Y Gillerot, et al.
Journal De Genetique Humaine
|
September 1, 1981
[Consanguineous marriages in genetic consultation]
M L Briard, J Kaplan, S Ayme, et al.
Page
of 5