Search research articles
Contact Us
Filters
Showing results (81-90 of 225) with videos related to
Page
of 23
Sort By:
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 phenotype
D Lacombe, A Toutain, R J Gorlin, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1995
Phenotypic variability in van der Woude syndrome
D 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) syndrome
A Lacalm, A Fichez, B Broussin, et al.
Human Genetics
|
April 1, 1998
Refined localisation of the voltage-gated chloride channel, CLCN3, to 4q33
L 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 bladder
E 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 syndrome
A 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 syndrome
D Lacombe, B Llanas, J F Chateil, et al.
Page
of 23
Search research articles
Search
Showing results (81-90 of 225) with videos related to
Sort By:
Page
of 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 phenotype
D Lacombe, A Toutain, R J Gorlin, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1995
Phenotypic variability in van der Woude syndrome
D 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) syndrome
A Lacalm, A Fichez, B Broussin, et al.
Human Genetics
|
April 1, 1998
Refined localisation of the voltage-gated chloride channel, CLCN3, to 4q33
L 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 bladder
E 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 syndrome
A 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 syndrome
D Lacombe, B Llanas, J F Chateil, et al.
Page
of 23