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Human Genetics
|
October 28, 1976
Possible intrachromosomal duplication in a case of trisomy 9p
H Chiyo, J Furuyama, N Suehara, et al.
Humangenetik
|
October 20, 1975
A 6p trisomy detected in a family with a "giant satellite"
H Chiyo, Y Kuroki, I Matsui, et al.
Journal of Oral and Maxillofacial Surgery : Official Journal of the American Association of Oral and Maxillofacial Surgeons
|
September 1, 1983
The oral manifestations of 4p- syndrome
M Morishita, R Shiba, H Chiyo, et al.
European Journal of Pediatrics
|
April 3, 1979
A case of neuraminidase deficiency associated with a partial beta-galactosidase defect. Clinical, biochemical and radiological studies
S Okada, T Yutaka, T Kato, et al.
Human Molecular Genetics
|
September 1, 1994
Monoallelic expression of normal mRNA in the PIT1 mutation heterozygotes with normal phenotype and biallelic expression in the abnormal phenotype
N Okamoto, Y Wada, S Ida, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 1, 1978
Hypersialyloligosacchariduria in mucolipidoses: a method for diagnosis
S Okada, T Kato, S Miura, et al.
Biochemical and Biophysical Research Communications
|
November 14, 1979
beta-Galactosidase deficient-type mucolipidosis: a complementation study of neuraminidase in somatic cell hybrids
T Kato, S Okada, T Yutaka, et al.
American Journal of Medical Genetics
|
September 11, 1995
Hereditary spherocytic anemia with deletion of the short arm of chromosome 8
N Okamoto, Y Wada, Y Nakamura, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
November 2, 2018
Increased Sylvian fissure angle as early sonographic sign of malformation of cortical development
R K Pooh, M Machida, T Nakamura, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Human Genetics
|
October 28, 1976
Possible intrachromosomal duplication in a case of trisomy 9p
H Chiyo, J Furuyama, N Suehara, et al.
Humangenetik
|
October 20, 1975
A 6p trisomy detected in a family with a "giant satellite"
H Chiyo, Y Kuroki, I Matsui, et al.
Journal of Oral and Maxillofacial Surgery : Official Journal of the American Association of Oral and Maxillofacial Surgeons
|
September 1, 1983
The oral manifestations of 4p- syndrome
M Morishita, R Shiba, H Chiyo, et al.
European Journal of Pediatrics
|
April 3, 1979
A case of neuraminidase deficiency associated with a partial beta-galactosidase defect. Clinical, biochemical and radiological studies
S Okada, T Yutaka, T Kato, et al.
Human Molecular Genetics
|
September 1, 1994
Monoallelic expression of normal mRNA in the PIT1 mutation heterozygotes with normal phenotype and biallelic expression in the abnormal phenotype
N Okamoto, Y Wada, S Ida, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 1, 1978
Hypersialyloligosacchariduria in mucolipidoses: a method for diagnosis
S Okada, T Kato, S Miura, et al.
Biochemical and Biophysical Research Communications
|
November 14, 1979
beta-Galactosidase deficient-type mucolipidosis: a complementation study of neuraminidase in somatic cell hybrids
T Kato, S Okada, T Yutaka, et al.
American Journal of Medical Genetics
|
September 11, 1995
Hereditary spherocytic anemia with deletion of the short arm of chromosome 8
N Okamoto, Y Wada, Y Nakamura, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
November 2, 2018
Increased Sylvian fissure angle as early sonographic sign of malformation of cortical development
R K Pooh, M Machida, T Nakamura, et al.
Page
of 2