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S Manouvrier

Showing results (31-40 of 79) with videos related to

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Prenatal Diagnosis|November 1, 1991
Prenatal diagnosis of PIBIDSJ B Savary, F Vasseur, D Vinatier, et al.
Annales De Pathologie|January 10, 2001
[Value of fetopathological examination in medical abortions: comparison of prenatal diagnosis and autopsy results of 300 fetuses]A Laussel-Riera, L Devisme, S Manouvrier-Hanu, et al.
Journal of Medical Genetics|December 1, 1996
Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25A Raas-Rothschild, S Manouvrier, M Gonzales, et al.
American Journal of Medical Genetics|December 1, 1989
Familial hyperinsulinism with nesidioblastosis of the pancreas: further evidence for autosomal recessive inheritanceL A Moreno, D Turck, F Gottrand, et al.
The British Journal of Dermatology|June 24, 2006
Phacomatosis pigmentokeratotica associated with hypophosphataemic rickets, pheochromocytoma and multiple basal cell carcinomasJ Bouthors, M-C Vantyghem, S Manouvrier-Hanu, et al.
American Journal of Medical Genetics|March 21, 1998
Blau syndrome of granulomatous arthritis, iritis, and skin rash: a new family and review of the literatureS Manouvrier-Hanu, B Puech, F Piette, et al.
Lancet (London, England)|August 25, 1990
Abnormal distribution of CF delta F508 allele in azoospermic men with congenital aplasia of epididymis and vas deferensV Dumur, R Gervais, J M Rigot, et al.
The New England Journal of Medicine|July 4, 1991
Cystic fibrosis and congenital absence of the vas deferensJ M Rigot, J J Lafitte, V Dumur, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Pulmonary hypertension of the newborn and urogenital anomalies in two male siblings: a new family with misalignment of pulmonary vesselsS Manouvrier-Hanu, L Devisme, I Farre, et al.
American Journal of Medical Genetics|March 29, 1996
Brachmann-de Lange syndrome: pre- and postnatal findingsS Manouvrier, M Espinasse, P Vaast, et al.
Pageof 8

Showing results (31-40 of 79) with videos related to

Sort By:
Pageof 8
Prenatal Diagnosis|November 1, 1991
Prenatal diagnosis of PIBIDSJ B Savary, F Vasseur, D Vinatier, et al.
Annales De Pathologie|January 10, 2001
[Value of fetopathological examination in medical abortions: comparison of prenatal diagnosis and autopsy results of 300 fetuses]A Laussel-Riera, L Devisme, S Manouvrier-Hanu, et al.
Journal of Medical Genetics|December 1, 1996
Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25A Raas-Rothschild, S Manouvrier, M Gonzales, et al.
American Journal of Medical Genetics|December 1, 1989
Familial hyperinsulinism with nesidioblastosis of the pancreas: further evidence for autosomal recessive inheritanceL A Moreno, D Turck, F Gottrand, et al.
The British Journal of Dermatology|June 24, 2006
Phacomatosis pigmentokeratotica associated with hypophosphataemic rickets, pheochromocytoma and multiple basal cell carcinomasJ Bouthors, M-C Vantyghem, S Manouvrier-Hanu, et al.
American Journal of Medical Genetics|March 21, 1998
Blau syndrome of granulomatous arthritis, iritis, and skin rash: a new family and review of the literatureS Manouvrier-Hanu, B Puech, F Piette, et al.
Lancet (London, England)|August 25, 1990
Abnormal distribution of CF delta F508 allele in azoospermic men with congenital aplasia of epididymis and vas deferensV Dumur, R Gervais, J M Rigot, et al.
The New England Journal of Medicine|July 4, 1991
Cystic fibrosis and congenital absence of the vas deferensJ M Rigot, J J Lafitte, V Dumur, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Pulmonary hypertension of the newborn and urogenital anomalies in two male siblings: a new family with misalignment of pulmonary vesselsS Manouvrier-Hanu, L Devisme, I Farre, et al.
American Journal of Medical Genetics|March 29, 1996
Brachmann-de Lange syndrome: pre- and postnatal findingsS Manouvrier, M Espinasse, P Vaast, et al.
Pageof 8