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Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|September 1, 1989
Micro extraction of DNA from whole blood and amniocytesT Hirota, T Kondoh, T Matsumoto, et al.Human Genetics|August 1, 1988
Origin of the extra chromosome in trisomy 18. A study on five patients using a restriction fragment length polymorphismT Kondoh, H Tonoki, T Matsumoto, et al.Journal of Human Genetics|February 4, 1999
Autosomal dominant onychodystrophy and congenital sensorineural deafnessT Kondoh, A Tsuru, T Matsumoto, et al.Journal of Human Genetics|June 4, 1998
New radiological finding by magnetic resonance imaging examination of the brain in Coffin-Lowry syndromeT Kondoh, T Matsumoto, M Ochi, et al.The Japanese Journal of Human Genetics|December 31, 2002
A nager acrofacial dysostosis syndrome patient with severe respiratory distress syndrome (RDS)T Kondoh, M Ito, A Ariyama, et al.Journal of Medical Genetics|May 5, 1999
47,XX,UPD(7)mat,+r(7)pat/46,XX,UPD(7)mat mosaicism in a girl with Silver-Russell syndrome (SRS): possible exclusion of the putative SRS gene from a 7p13-q11 regionO Miyoshi, T Kondoh, H Taneda, et al.Bone Marrow Transplantation|November 25, 1998
Complete-type DiGeorge syndrome treated by bone marrow transplantationT Matsumoto, N Amamoto, T Kondoh, et al.Acta Paediatrica Japonica : Overseas Edition|February 1, 1991
Deletion pattern in the 21-hydroxylase gene detected by polymerase chain reactionE Kinoshita, T Matsumoto, T Kondoh, et al.American Journal of Medical Genetics|July 27, 2001
Condition of microcephaly, growth retardation, joint contractures, atopic dermatitis, and mental retardation in two Japanese sisters: a new autosomal recessive MCA/MR syndrome?T Kondoh, T Yamamoto, Y Kono, et al.American Journal of Medical Genetics|October 9, 1995
Two sisters with clinical diagnosis of Wiskott-Aldrich syndrome: is the condition in the family autosomal recessive?T Kondoh, K Hayashi, T Matsumoto, et al.Pageof 271