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D Lacombe

Showing results (81-90 of 225) with videos related to

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Revue De Laryngologie - Otologie - Rhinologie|January 1, 1997
[ORL and speech aspects in DiGeorge syndrome]D Portmann, M Marraco, D Lacombe, et al.
Annales De Genetique|January 1, 1994
Clinical identification of a human equivalent to the short ear (se) murine phenotypeD Lacombe, A Toutain, R J Gorlin, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Phenotypic variability in van der Woude syndromeD Lacombe, J M Pedespan, D Fontan, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 16, 2017
Prenatal diagnosis of cerebral and extracerebral high-flow lesions revealing familial capillary malformation-arteriovenous malformation (CM-AVM) syndromeA Lacalm, A Fichez, B Broussin, et al.
Human Genetics|April 1, 1998
Refined localisation of the voltage-gated chloride channel, CLCN3, to 4q33L Taine, I Coupry, P Boisseau, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 1, 1996
[Microdeletion of the chromosome 22q11 in children: apropos of a series of 49 patients]A Levy-Mozziconacci, D Lacombe, B Leheup, et al.
Genetic Counseling (Geneva, Switzerland)|November 3, 2004
Trisomy 22 with thyroid isthmus agenesis and absent gall bladderE Gangbo, D Lacombe, E M Alberti, et al.
American Journal of Medical Genetics. Part A|February 24, 2007
Oro-dental features as useful diagnostic tool in Rubinstein-Taybi syndromeA Bloch-Zupan, J Stachtou, D Emmanouil, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1997
[Does germinal chromosomal mosaicism exist?]C Goizet, L Taine, Z Q Wen, et al.
Clinical Dysmorphology|October 1, 1994
Severe presentation of Peters'-Plus syndromeD Lacombe, B Llanas, J F Chateil, et al.
Pageof 23

Showing results (81-90 of 225) with videos related to

Sort By:
Pageof 23
Revue De Laryngologie - Otologie - Rhinologie|January 1, 1997
[ORL and speech aspects in DiGeorge syndrome]D Portmann, M Marraco, D Lacombe, et al.
Annales De Genetique|January 1, 1994
Clinical identification of a human equivalent to the short ear (se) murine phenotypeD Lacombe, A Toutain, R J Gorlin, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Phenotypic variability in van der Woude syndromeD Lacombe, J M Pedespan, D Fontan, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 16, 2017
Prenatal diagnosis of cerebral and extracerebral high-flow lesions revealing familial capillary malformation-arteriovenous malformation (CM-AVM) syndromeA Lacalm, A Fichez, B Broussin, et al.
Human Genetics|April 1, 1998
Refined localisation of the voltage-gated chloride channel, CLCN3, to 4q33L Taine, I Coupry, P Boisseau, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 1, 1996
[Microdeletion of the chromosome 22q11 in children: apropos of a series of 49 patients]A Levy-Mozziconacci, D Lacombe, B Leheup, et al.
Genetic Counseling (Geneva, Switzerland)|November 3, 2004
Trisomy 22 with thyroid isthmus agenesis and absent gall bladderE Gangbo, D Lacombe, E M Alberti, et al.
American Journal of Medical Genetics. Part A|February 24, 2007
Oro-dental features as useful diagnostic tool in Rubinstein-Taybi syndromeA Bloch-Zupan, J Stachtou, D Emmanouil, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1997
[Does germinal chromosomal mosaicism exist?]C Goizet, L Taine, Z Q Wen, et al.
Clinical Dysmorphology|October 1, 1994
Severe presentation of Peters'-Plus syndromeD Lacombe, B Llanas, J F Chateil, et al.
Pageof 23