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Paediatrician
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January 1, 1979
Gram-negative germs infections in infancy
J M Corretger, E Sánchez, S Uríz, et al.
Anales Espanoles De Pediatria
|
August 1, 1986
[Dermatoglyphic studies in parents of children with Down's syndrome. I. Digital patterns]
A de Izuzquiza Uriszar-Aldaca, C Ascaso Terrén, F Ballesta Martínez
Journal of Medical Genetics
|
May 5, 1999
Trisomy/tetrasomy 21 mosaicism in CVS: interpretation of cytogenetic discrepancies between placental and fetal chromosome complements
A Soler, E Margarit, A Carrió, et al.
American Journal of Human Genetics
|
March 1, 1994
Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twins
H Kruyer, M Milà, G Glover, et al.
Pediatric Dermatology
|
January 22, 1998
Trichothiodystrophy associated with urologic malformation and primary hypercalciuria
J Malvehy, J Ferrando, J Soler, et al.
Human Genetics
|
January 1, 1990
Meiotic and sperm chromosome studies in a reciprocal translocation t(1;2)(q32;q36)
C Templado, J Navarro, R Requena, et al.
Anales Espanoles De Pediatria
|
April 1, 1979
[Male pseudohermaphroditism due to deficit in the conversion of cholesterol to delta5 pregnenolone (author's transl)]
F R Hierro, A Orús, J M Corretger, et al.
Anales Espanoles De Pediatria
|
November 1, 1981
[Hyperinsulinism and peripheral resistance to insulin in a case of leprechaunism]
N Lambruschini, J M Barguñó, C Villanueva, et al.
Journal of Hepatology
|
December 2, 1998
Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls
M Sánchez, M Bruguera, J Bosch, et al.
Anales Espanoles De Pediatria
|
June 1, 1976
[Myelomonocytic leukemia in childhood (author's transl)]
E Vela Ferrer, F Ballesta Martínez, J A Molina Font, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 70) with videos related to
Sort By:
Page
of 7
Paediatrician
|
January 1, 1979
Gram-negative germs infections in infancy
J M Corretger, E Sánchez, S Uríz, et al.
Anales Espanoles De Pediatria
|
August 1, 1986
[Dermatoglyphic studies in parents of children with Down's syndrome. I. Digital patterns]
A de Izuzquiza Uriszar-Aldaca, C Ascaso Terrén, F Ballesta Martínez
Journal of Medical Genetics
|
May 5, 1999
Trisomy/tetrasomy 21 mosaicism in CVS: interpretation of cytogenetic discrepancies between placental and fetal chromosome complements
A Soler, E Margarit, A Carrió, et al.
American Journal of Human Genetics
|
March 1, 1994
Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twins
H Kruyer, M Milà, G Glover, et al.
Pediatric Dermatology
|
January 22, 1998
Trichothiodystrophy associated with urologic malformation and primary hypercalciuria
J Malvehy, J Ferrando, J Soler, et al.
Human Genetics
|
January 1, 1990
Meiotic and sperm chromosome studies in a reciprocal translocation t(1;2)(q32;q36)
C Templado, J Navarro, R Requena, et al.
Anales Espanoles De Pediatria
|
April 1, 1979
[Male pseudohermaphroditism due to deficit in the conversion of cholesterol to delta5 pregnenolone (author's transl)]
F R Hierro, A Orús, J M Corretger, et al.
Anales Espanoles De Pediatria
|
November 1, 1981
[Hyperinsulinism and peripheral resistance to insulin in a case of leprechaunism]
N Lambruschini, J M Barguñó, C Villanueva, et al.
Journal of Hepatology
|
December 2, 1998
Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls
M Sánchez, M Bruguera, J Bosch, et al.
Anales Espanoles De Pediatria
|
June 1, 1976
[Myelomonocytic leukemia in childhood (author's transl)]
E Vela Ferrer, F Ballesta Martínez, J A Molina Font, et al.
Page
of 7