F de Luca|J L Chaussain|J C Job - JoVE Visualize

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La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|October 8, 1981

[Puberty and adult height in congenital virilizing adrenal hyperplasia (author's transl)]F Himon, J C Job, M Pierson, et al.

Archives Francaises De Pediatrie|December 1, 1981

[Epidemiology of hypothyroidism due to congenital malformation of the gland: athyreosis or ectopic thyroid (author's transl)]J Goujard, A Safar, A Rolland, et al.

Acta Endocrinologica|June 1, 1978

Correlative study of radioreceptor assay and radioimmunoassay of serum growth hormone in children. II: Primary, genetic and intra-uterine growth retardationP E Garnier, A M Repellin, J C Job

Annales D'Endocrinologie|January 1, 1989

[Elevated levels of plasma 4-ene steroids in a case of congenital deficiency of 3 beta-hydroxysteroid dehydrogenase]K Nahoul, C Perrin, P Leymarie, et al.

Gene|May 8, 1996

A silent trans-splicing signal in the cuticlin-encoding gene of the plant-parasitic nematode Meloidogyne artielliaC De Giorgi, F De Luca, F Lamberti

Molecular Genetics and Metabolism|August 28, 1998

Activating mutations of the Ca2+-sensing receptorE E Mancilla, F De Luca, J Baron

Gene|July 22, 1991

Mitochondrial DNA in the sea urchin Arbacia lixula: nucleotide sequence differences between two polymorphic molecules indicate asymmetry of mutationsC De Giorgi, F De Luca, C Saccone

Helvetica Paediatrica Acta|June 1, 1987

Obesity in a child with untreated coeliac diseaseS Conti Nibali, G Magazzù, F De Luca

American Journal of Human Genetics|June 1, 1996

A novel mutation in the putative DNA helicase XH2 is responsible for male-to-female sex reversal associated with an atypical form of the ATR-X syndromeA Ion, L Telvi, J L Chaussain, et al.

The Journal of Clinical Endocrinology and Metabolism|August 1, 1996

Different phenotypes in a family with androgen insensitivity caused by the same M780I point mutation in the androgen receptor geneP Rodien, F Mebarki, I Mowszowicz, et al.

Pageof 51

Showing results (181-190 of 502) with videos related to

Sort By:

Pageof 51

La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|October 8, 1981

[Puberty and adult height in congenital virilizing adrenal hyperplasia (author's transl)]F Himon, J C Job, M Pierson, et al.

Archives Francaises De Pediatrie|December 1, 1981

[Epidemiology of hypothyroidism due to congenital malformation of the gland: athyreosis or ectopic thyroid (author's transl)]J Goujard, A Safar, A Rolland, et al.

Acta Endocrinologica|June 1, 1978

Correlative study of radioreceptor assay and radioimmunoassay of serum growth hormone in children. II: Primary, genetic and intra-uterine growth retardationP E Garnier, A M Repellin, J C Job

Annales D'Endocrinologie|January 1, 1989

[Elevated levels of plasma 4-ene steroids in a case of congenital deficiency of 3 beta-hydroxysteroid dehydrogenase]K Nahoul, C Perrin, P Leymarie, et al.

Gene|May 8, 1996

A silent trans-splicing signal in the cuticlin-encoding gene of the plant-parasitic nematode Meloidogyne artielliaC De Giorgi, F De Luca, F Lamberti

Molecular Genetics and Metabolism|August 28, 1998

Activating mutations of the Ca2+-sensing receptorE E Mancilla, F De Luca, J Baron

Gene|July 22, 1991

Mitochondrial DNA in the sea urchin Arbacia lixula: nucleotide sequence differences between two polymorphic molecules indicate asymmetry of mutationsC De Giorgi, F De Luca, C Saccone

Helvetica Paediatrica Acta|June 1, 1987

Obesity in a child with untreated coeliac diseaseS Conti Nibali, G Magazzù, F De Luca

American Journal of Human Genetics|June 1, 1996

A novel mutation in the putative DNA helicase XH2 is responsible for male-to-female sex reversal associated with an atypical form of the ATR-X syndromeA Ion, L Telvi, J L Chaussain, et al.

The Journal of Clinical Endocrinology and Metabolism|August 1, 1996

Different phenotypes in a family with androgen insensitivity caused by the same M780I point mutation in the androgen receptor geneP Rodien, F Mebarki, I Mowszowicz, et al.

Pageof 51