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J C Lambert

Showing results (21-30 of 112) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 30, 2005
[ATR-X syndrome: a new mutation in the XNP/ATRX gene near the helicase domain]F Giuliano, C Badens, C Richelme, et al.
Human Genetics|April 17, 1979
18Q - syndrome resulting from a tdic(14p; 18q)J C Lambert, M Ferrari, C Bergondi, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 9, 2002
Harlequin fetus: three-dimensional sonographic findings and new diagnostic approachA Bongain, B Benoit, L Ejnes, et al.
Journal of Medical Genetics|February 1, 1984
Triploidy with cyclopia and identical HLA alleles in the parentsJ C Lambert, P Philip, G Charpentier, et al.
Archives Francaises De Pediatrie|March 1, 1981
[Monosomy 7qter (author's transl)]J C Lambert, R Mariani, M Donzeau, et al.
Human Genetics|January 1, 1981
Arthrogryposis-like signs in trisomy 18J C Lambert, M Ferrari, M Donzeau, et al.
Journal of Medical Genetics|June 1, 1982
Familial occurrence of a syndrome with branchial dysplasia, mental deficiency, club feet, and inguinal herniaeJ C Lambert, N Ayraud, J Martin, et al.
Tissue Antigens|February 1, 1985
HLA in families with Down's syndrome childrenP Soubiran, S Benzaken, J Piereschi, et al.
Clinical Dysmorphology|November 21, 1998
Congenital bowing of the long bones in two fetuses presenting features of Stüve-Wiedemann syndrome and Schwartz-Jampel syndrome type 2S Sigaudy, A Moncla, C Fredouille, et al.
Lancet (London, England)|June 23, 1998
Association at LRP gene locus with sporadic late-onset Alzheimer's diseaseJ C Lambert, F Wavrant-De Vrièze, P Amouyel, et al.
Pageof 12

Showing results (21-30 of 112) with videos related to

Sort By:
Pageof 12
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 30, 2005
[ATR-X syndrome: a new mutation in the XNP/ATRX gene near the helicase domain]F Giuliano, C Badens, C Richelme, et al.
Human Genetics|April 17, 1979
18Q - syndrome resulting from a tdic(14p; 18q)J C Lambert, M Ferrari, C Bergondi, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 9, 2002
Harlequin fetus: three-dimensional sonographic findings and new diagnostic approachA Bongain, B Benoit, L Ejnes, et al.
Journal of Medical Genetics|February 1, 1984
Triploidy with cyclopia and identical HLA alleles in the parentsJ C Lambert, P Philip, G Charpentier, et al.
Archives Francaises De Pediatrie|March 1, 1981
[Monosomy 7qter (author's transl)]J C Lambert, R Mariani, M Donzeau, et al.
Human Genetics|January 1, 1981
Arthrogryposis-like signs in trisomy 18J C Lambert, M Ferrari, M Donzeau, et al.
Journal of Medical Genetics|June 1, 1982
Familial occurrence of a syndrome with branchial dysplasia, mental deficiency, club feet, and inguinal herniaeJ C Lambert, N Ayraud, J Martin, et al.
Tissue Antigens|February 1, 1985
HLA in families with Down's syndrome childrenP Soubiran, S Benzaken, J Piereschi, et al.
Clinical Dysmorphology|November 21, 1998
Congenital bowing of the long bones in two fetuses presenting features of Stüve-Wiedemann syndrome and Schwartz-Jampel syndrome type 2S Sigaudy, A Moncla, C Fredouille, et al.
Lancet (London, England)|June 23, 1998
Association at LRP gene locus with sporadic late-onset Alzheimer's diseaseJ C Lambert, F Wavrant-De Vrièze, P Amouyel, et al.
Pageof 12