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A Nivelon

Showing results (21-30 of 48) with videos related to

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Neurophysiologie Clinique = Clinical Neurophysiology|March 1, 1989
[Familial benign neonatal seizures: EEG, clinical, prognosis and genetic features]M Giroud, P Soichot, A Nivelon-Chevalier, et al.
Archives Francaises De Pediatrie|December 1, 1987
[Treatment of citrullinemia. Apropos of a case followed from birth. Importance of alpha-ketonic acids]D Tenenbaum, A M Petion, J Desgres, et al.
Journal De Genetique Humaine|June 1, 1985
[Prenatal diagnosis in a familial form of male pseudohermaphroditism due to 17-keto reductase deficiency]J L Nivelon, M G Forest, A Nivelon-Chevallier, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1991
[Retrocervical cystic hygroma: diagnosis, prognosis and management. A series of 13 cases]S Douvier, J P Feldman, A Nivelon-Chevalier, et al.
Journal of Medical Genetics|August 28, 1999
Hydrometrocolpos and polydactyly: a common neonatal presentation of Bardet-Biedl and McKusick-Kaufman syndromesA David, P Bitoun, D Lacombe, et al.
Human Genetics|August 1, 1995
A gene for blepharophimosis-ptosis-epicanthus inversus syndrome maps to chromosome 3q23P Amati, J C Chomel, A Nivelon-Chevalier, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1980
[Gonad function of women with homogenous karyotype XO or with mosaic form. Five case histories of fertile women (author's transl)]A Mavel, C Turc, J P Feldman, et al.
Annales De Pediatrie|September 1, 1993
[Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 9 treated pregnancies]J L Nivelon, M Chouchane, M G Forest, et al.
Clinical Dysmorphology|October 1, 1992
New autosomal recessive chondrodysplasia--pseudohermaphrodism syndromeA Nivelon, J L Nivelon, J P Mabille, et al.
Prenatal Diagnosis|July 5, 2001
Familial orofaciodigital syndrome type I revealed by ultrasound prenatal diagnosis of porencephalyC Thauvin-Robinet, T Rousseau, C Durand, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Neurophysiologie Clinique = Clinical Neurophysiology|March 1, 1989
[Familial benign neonatal seizures: EEG, clinical, prognosis and genetic features]M Giroud, P Soichot, A Nivelon-Chevalier, et al.
Archives Francaises De Pediatrie|December 1, 1987
[Treatment of citrullinemia. Apropos of a case followed from birth. Importance of alpha-ketonic acids]D Tenenbaum, A M Petion, J Desgres, et al.
Journal De Genetique Humaine|June 1, 1985
[Prenatal diagnosis in a familial form of male pseudohermaphroditism due to 17-keto reductase deficiency]J L Nivelon, M G Forest, A Nivelon-Chevallier, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1991
[Retrocervical cystic hygroma: diagnosis, prognosis and management. A series of 13 cases]S Douvier, J P Feldman, A Nivelon-Chevalier, et al.
Journal of Medical Genetics|August 28, 1999
Hydrometrocolpos and polydactyly: a common neonatal presentation of Bardet-Biedl and McKusick-Kaufman syndromesA David, P Bitoun, D Lacombe, et al.
Human Genetics|August 1, 1995
A gene for blepharophimosis-ptosis-epicanthus inversus syndrome maps to chromosome 3q23P Amati, J C Chomel, A Nivelon-Chevalier, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1980
[Gonad function of women with homogenous karyotype XO or with mosaic form. Five case histories of fertile women (author's transl)]A Mavel, C Turc, J P Feldman, et al.
Annales De Pediatrie|September 1, 1993
[Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 9 treated pregnancies]J L Nivelon, M Chouchane, M G Forest, et al.
Clinical Dysmorphology|October 1, 1992
New autosomal recessive chondrodysplasia--pseudohermaphrodism syndromeA Nivelon, J L Nivelon, J P Mabille, et al.
Prenatal Diagnosis|July 5, 2001
Familial orofaciodigital syndrome type I revealed by ultrasound prenatal diagnosis of porencephalyC Thauvin-Robinet, T Rousseau, C Durand, et al.
Pageof 5