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10,207 results

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Page 1
Condition of microcephaly, growth retardation, joint contractures, atopic dermatitis, and mental retardation in two Japanese sisters: a new autosomal recessive MCA/MR syndrome?
Kondoh T, Yamamoto T, Kono Y, Matsumoto T, Sugawara H, Matsumoto N, Moriuchi H. Kondoh T, et al. Among authors: matsumoto n, matsumoto t. Am J Med Genet. 2001 Jul 22;102(1):63-7. doi: 10.1002/1096-8628(20010722)102:1<63::aid-ajmg1415>3.0.co;2-u. Am J Med Genet. 2001. PMID: 11471174
Wiskott-Aldrich syndrome in two sisters.
Kondoh T, Matsumoto T, Tsuji Y. Kondoh T, et al. Among authors: matsumoto t. Am J Med Genet. 1997 Apr 18;74(2):218-9. doi: 10.1002/(sici)1096-8628(19970418)74:2<218::aid-ajmg23>3.0.co;2-k. Am J Med Genet. 1997. PMID: 9129730 No abstract available.
[Neu-Laxova syndrome].
Kondoh T, Matsumoto T. Kondoh T, et al. Among authors: matsumoto t. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):283-4. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528742 Review. Japanese. No abstract available.
[Neuroectodermal melanolysosomal syndrome].
Kondoh T, Matsumoto T. Kondoh T, et al. Among authors: matsumoto t. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):289-90. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528745 Review. Japanese. No abstract available.
[Neuro-facio-digito-renal syndrome].
Kondoh T, Matsumoto T. Kondoh T, et al. Among authors: matsumoto t. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):293-4. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528747 Review. Japanese. No abstract available.
[Nevo syndrome].
Kondoh T, Matsumoto T. Kondoh T, et al. Among authors: matsumoto t. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):311-2. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528757 Review. Japanese. No abstract available.
[Raine syndrome].
Kondoh T, Matsumoto T. Kondoh T, et al. Among authors: matsumoto t. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):569-70. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528901 Review. Japanese. No abstract available.
10,207 results
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