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Neuromuscular Disorders : NMD
|
January 1, 1992
Immunoquantitation of carnitine palmitoyl transferase in skeletal muscle of 31 patients
G D Vladutiu, I Saponara, J M Conroy, et al.
The Journal of Nutrition
|
October 1, 1989
Evaluation of vitamin B-6 status and function of rats fed excess pyridoxine
M C Schaeffer, D A Sampson, J H Skala, et al.
Annals of Neurology
|
November 1, 1985
Biotinidase deficiency: initial clinical features and rapid diagnosis
B Wolf, G S Heard, K A Weissbecker, et al.
The Journal of Pediatrics
|
August 1, 1983
Phenotypic variation in biotinidase deficiency
B Wolf, R E Grier, R J Allen, et al.
Prenatal Diagnosis
|
August 1, 1996
Triple marker screening in native Japanese women
T Onda, M Kitagawa, O Takeda, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 5, 2001
Technical standards and guidelines for fragile X: the first of a series of disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics. Quality Assurance Subcommittee of the Laboratory Practice Committee
A Maddalena, C S Richards, M J McGinniss, et al.
Prenatal Diagnosis
|
August 19, 1999
Amniotic fluid alpha-fetoprotein testing in native Japanese women
T Onda, K Fukushima, T Tanaka, et al.
The Journal of Obstetrics and Gynaecology Research
|
August 10, 2000
Dimeric inhibin A as a fourth marker for Down's syndrome maternal serum screening in native Japanese women
K Yoshida, Y Kuwabara, T Tanaka, et al.
The Journal of Obstetrics and Gynaecology Research
|
January 11, 2001
Triple marker screening for trisomy 21, trisomy 18 and open neural tube defects in singleton pregnancies of native Japanese pregnant women
T Onda, T Tanaka, K Yoshida, et al.
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of 2
Search research articles
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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.
Neuromuscular Disorders : NMD
|
January 1, 1992
Immunoquantitation of carnitine palmitoyl transferase in skeletal muscle of 31 patients
G D Vladutiu, I Saponara, J M Conroy, et al.
The Journal of Nutrition
|
October 1, 1989
Evaluation of vitamin B-6 status and function of rats fed excess pyridoxine
M C Schaeffer, D A Sampson, J H Skala, et al.
Annals of Neurology
|
November 1, 1985
Biotinidase deficiency: initial clinical features and rapid diagnosis
B Wolf, G S Heard, K A Weissbecker, et al.
The Journal of Pediatrics
|
August 1, 1983
Phenotypic variation in biotinidase deficiency
B Wolf, R E Grier, R J Allen, et al.
Prenatal Diagnosis
|
August 1, 1996
Triple marker screening in native Japanese women
T Onda, M Kitagawa, O Takeda, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 5, 2001
Technical standards and guidelines for fragile X: the first of a series of disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics. Quality Assurance Subcommittee of the Laboratory Practice Committee
A Maddalena, C S Richards, M J McGinniss, et al.
Prenatal Diagnosis
|
August 19, 1999
Amniotic fluid alpha-fetoprotein testing in native Japanese women
T Onda, K Fukushima, T Tanaka, et al.
The Journal of Obstetrics and Gynaecology Research
|
August 10, 2000
Dimeric inhibin A as a fourth marker for Down's syndrome maternal serum screening in native Japanese women
K Yoshida, Y Kuwabara, T Tanaka, et al.
The Journal of Obstetrics and Gynaecology Research
|
January 11, 2001
Triple marker screening for trisomy 21, trisomy 18 and open neural tube defects in singleton pregnancies of native Japanese pregnant women
T Onda, T Tanaka, K Yoshida, et al.
Page
of 2