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Clinical Genetics
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February 1, 1987
Inv(4)(p16q21). A five-generation pedigree with 24 carriers and no recombinants
F Rivas, L García-Esquivel, H Rivera, et al.
Annales De Genetique
|
January 1, 1994
Paternal non-disjunction evidenced by G6PD electrophoretic phenotypes in a 48,XXXY patient
C Medina, G Zuñiga, G Ramirez, et al.
Annales De Genetique
|
January 1, 1996
Alphoidless centromere of a familial unstable inverted Y chromosome
H Rivera, A I Vassquez, M L Ayala-Madrigal, et al.
American Journal of Medical Genetics
|
April 1, 1985
Azoospermia and duplication 3qter as distinct consequences of a familial t(X;3) (q26;q13.2)
J M Cantú, M Díaz, M Möller, et al.
Genetic Counseling (Geneva, Switzerland)
|
August 4, 2004
Sensorineural deafness in two infants: a novel feature in the 22q distal duplication syndrome. Cardinal signs in trisomies 22 subtypes
L O Barajas-Barajas, L L Valdez, J R Gonzalez, et al.
Journal De Genetique Humaine
|
December 1, 1983
Del (8) (q212q2200) de novo in a boy without Langer-Giedion syndrome
H Rivera, R M Rodríguez, M L Plascencia, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion
|
April 1, 1985
[Chromosome aberrations in 334 individuals with various types of abortion (including 144 couples)]
J M Cantú, A Hernández, M Jiménez-Sáinz, et al.
Annales De Genetique
|
January 1, 1981
Simultaneous trisomy 10q24 leads to qter and monosomy 4p16: an example of epistasis at the chromosome level
J M Cantu, A Hernandez, Z Nazara, et al.
Panminerva Medica
|
March 12, 2002
New concept regarding chest pain due to hypoxia of the internal mammary arteries in more than 1,600 operated patients with cerebral thoracic neurovascular syndrome (CTNVS)
E I Fernandez Noda, H Rivera Luna, J Perez Fernandez, et al.
Journal De Genetique Humaine
|
August 1, 1986
Autosomal dominant piebaldism and mental retardation syndrome associated with a t(1;2) (p22.1;q36)
H Rivera, M C Alvarez-Arratia, M Moller, et al.
Page
of 28
Search research articles
Search
Showing results (201-210 of 275) with videos related to
Sort By:
Page
of 28
Clinical Genetics
|
February 1, 1987
Inv(4)(p16q21). A five-generation pedigree with 24 carriers and no recombinants
F Rivas, L García-Esquivel, H Rivera, et al.
Annales De Genetique
|
January 1, 1994
Paternal non-disjunction evidenced by G6PD electrophoretic phenotypes in a 48,XXXY patient
C Medina, G Zuñiga, G Ramirez, et al.
Annales De Genetique
|
January 1, 1996
Alphoidless centromere of a familial unstable inverted Y chromosome
H Rivera, A I Vassquez, M L Ayala-Madrigal, et al.
American Journal of Medical Genetics
|
April 1, 1985
Azoospermia and duplication 3qter as distinct consequences of a familial t(X;3) (q26;q13.2)
J M Cantú, M Díaz, M Möller, et al.
Genetic Counseling (Geneva, Switzerland)
|
August 4, 2004
Sensorineural deafness in two infants: a novel feature in the 22q distal duplication syndrome. Cardinal signs in trisomies 22 subtypes
L O Barajas-Barajas, L L Valdez, J R Gonzalez, et al.
Journal De Genetique Humaine
|
December 1, 1983
Del (8) (q212q2200) de novo in a boy without Langer-Giedion syndrome
H Rivera, R M Rodríguez, M L Plascencia, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion
|
April 1, 1985
[Chromosome aberrations in 334 individuals with various types of abortion (including 144 couples)]
J M Cantú, A Hernández, M Jiménez-Sáinz, et al.
Annales De Genetique
|
January 1, 1981
Simultaneous trisomy 10q24 leads to qter and monosomy 4p16: an example of epistasis at the chromosome level
J M Cantu, A Hernandez, Z Nazara, et al.
Panminerva Medica
|
March 12, 2002
New concept regarding chest pain due to hypoxia of the internal mammary arteries in more than 1,600 operated patients with cerebral thoracic neurovascular syndrome (CTNVS)
E I Fernandez Noda, H Rivera Luna, J Perez Fernandez, et al.
Journal De Genetique Humaine
|
August 1, 1986
Autosomal dominant piebaldism and mental retardation syndrome associated with a t(1;2) (p22.1;q36)
H Rivera, M C Alvarez-Arratia, M Moller, et al.
Page
of 28