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81.
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A fine physical map of Arabidopsis thaliana chromosome 5: construction of a sequence-ready contig map. [electronic resource] by
- Kotani, H
- Sato, S
- Fukami, M
- Hosouchi, T
- Nakazaki, N
- Okumura, S
- Wada, T
- Liu, Y G
- Shibata, D
- Tabata, S
Producer: 19980428
In:
DNA research : an international journal for rapid publication of reports on genes and genomes vol. 4
Availability: No items available.
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82.
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Copy number variations in the amylase gene (AMY2B) in Japanese native dog breeds. [electronic resource] by
- Tonoike, A
- Hori, Y
- Inoue-Murayama, M
- Konno, A
- Fujita, K
- Miyado, M
- Fukami, M
- Nagasawa, M
- Mogi, K
- Kikusui, T
Producer: 20151224
In:
Animal genetics vol. 46
Availability: No items available.
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83.
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FISH-deletion mapping defines a 270-kb short stature critical interval in the pseudoautosomal region PAR1 on human sex chromosomes. [electronic resource] by
- Rao, E
- Weiss, B
- Fukami, M
- Mertz, A
- Meder, J
- Ogata, T
- Heinrich, U
- Garcia-Heras, J
- Schiebel, K
- Rappold, G A
Producer: 19970908
In:
Human genetics vol. 100
Availability: No items available.
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84.
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Phenotypic variation and genetic heterogeneity in Léri-Weill syndrome. [electronic resource] by
- Schiller, S
- Spranger, S
- Schechinger, B
- Fukami, M
- Merker, S
- Drop, S L
- Tröger, J
- Knoblauch, H
- Kunze, J
- Seidel, J
- Rappold, G A
Producer: 20000414
In:
European journal of human genetics : EJHG vol. 8
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85.
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Low prevalence of maternal microchimerism in peripheral blood of Japanese children with type 1 diabetes. [electronic resource] by
- Ushijima, K
- Okuno, M
- Ayabe, T
- Kikuchi, N
- Kawamura, T
- Urakami, T
- Yokota, I
- Amemiya, S
- Uchiyama, T
- Kikuchi, T
- Ogata, T
- Sugihara, S
- Fukami, M
Producer: 20211029
In:
Diabetic medicine : a journal of the British Diabetic Association vol. 37
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86.
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A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation. [electronic resource] by
- Fukami, M
- Kirsch, S
- Schiller, S
- Richter, A
- Benes, V
- Franco, B
- Muroya, K
- Rao, E
- Merker, S
- Niesler, B
- Ballabio, A
- Ansorge, W
- Ogata, T
- Rappold, G A
Producer: 20000919
In:
American journal of human genetics vol. 67
Availability: No items available.
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87.
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Next-generation sequencing for patients with non-obstructive azoospermia: implications for significant roles of monogenic/oligogenic mutations. [electronic resource] by
- Nakamura, S
- Miyado, M
- Saito, K
- Katsumi, M
- Nakamura, A
- Kobori, Y
- Tanaka, Y
- Ishikawa, H
- Yoshida, A
- Okada, H
- Hata, K
- Nakabayashi, K
- Okamura, K
- Ogata, H
- Matsubara, Y
- Ogata, T
- Nakai, H
- Fukami, M
Producer: 20180129
In:
Andrology vol. 5
Availability: No items available.
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88.
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Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome. [electronic resource] by
- Rao, E
- Weiss, B
- Fukami, M
- Rump, A
- Niesler, B
- Mertz, A
- Muroya, K
- Binder, G
- Kirsch, S
- Winkelmann, M
- Nordsiek, G
- Heinrich, U
- Breuning, M H
- Ranke, M B
- Rosenthal, A
- Ogata, T
- Rappold, G A
Producer: 19970616
In:
Nature genetics vol. 16
Availability: No items available.
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89.
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Polymorphisms of MAMLD1 gene in hypospadias. [electronic resource] by
- Kalfa, N
- Cassorla, F
- Audran, F
- Oulad Abdennabi, I
- Philibert, P
- Béroud, C
- Guys, J M
- Reynaud, R
- Alessandrini, P
- Wagner, K
- Bréaud, J
- Valla, J S
- Morisson Lacombe, G
- Daures, J P
- Baskin, L
- Fukami, M
- Ogata, T
- Sultan, C
Producer: 20120412
In:
Journal of pediatric urology vol. 7
Availability: No items available.
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90.
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Protein-altering variants of PTPN2 in childhood-onset Type 1A diabetes. [electronic resource] by
- Okuno, M
- Ayabe, T
- Yokota, I
- Musha, I
- Shiga, K
- Kikuchi, T
- Kikuchi, N
- Ohtake, A
- Nakamura, A
- Nakabayashi, K
- Okamura, K
- Momozawa, Y
- Kubo, M
- Suzuki, J
- Urakami, T
- Kawamura, T
- Amemiya, S
- Ogata, T
- Sugihara, S
- Fukami, M
Producer: 20181217
In:
Diabetic medicine : a journal of the British Diabetic Association vol. 35
Availability: No items available.
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91.
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Molecular basis of non-syndromic hypospadias: systematic mutation screening and genome-wide copy-number analysis of 62 patients. [electronic resource] by
- Kon, M
- Suzuki, E
- Dung, V C
- Hasegawa, Y
- Mitsui, T
- Muroya, K
- Ueoka, K
- Igarashi, N
- Nagasaki, K
- Oto, Y
- Hamajima, T
- Yoshino, K
- Igarashi, M
- Kato-Fukui, Y
- Nakabayashi, K
- Hayashi, K
- Hata, K
- Matsubara, Y
- Moriya, K
- Ogata, T
- Nonomura, K
- Fukami, M
Producer: 20151109
In:
Human reproduction (Oxford, England) vol. 30
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92.
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Variants associated with autoimmune Type 1 diabetes in Japanese children: implications for age-specific effects of cis-regulatory haplotypes at 17q12-q21. [electronic resource] by
- Ayabe, T
- Fukami, M
- Ogata, T
- Kawamura, T
- Urakami, T
- Kikuchi, N
- Yokota, I
- Ihara, K
- Takemoto, K
- Mukai, T
- Nishii, A
- Kikuchi, T
- Mori, T
- Shimura, N
- Sasaki, G
- Kizu, R
- Takubo, N
- Soneda, S
- Fujisawa, T
- Takaya, R
- Kizaki, Z
- Kanzaki, S
- Hanaki, K
- Matsuura, N
- Kasahara, Y
- Kosaka, K
- Takahashi, T
- Minamitani, K
- Matsuo, S
- Mochizuki, H
- Kobayashi, K
- Koike, A
- Horikawa, R
- Teno, S
- Tsubouchi, K
- Mochizuki, T
- Igarashi, Y
- Amemiya, S
- Sugihara, S
Producer: 20180109
In:
Diabetic medicine : a journal of the British Diabetic Association vol. 33
Availability: No items available.
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93.
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FUT2 non-secretor status is associated with Type 1 diabetes susceptibility in Japanese children. [electronic resource] by
- Ihara, K
- Fukano, C
- Ayabe, T
- Fukami, M
- Ogata, T
- Kawamura, T
- Urakami, T
- Kikuchi, N
- Yokota, I
- Takemoto, K
- Mukai, T
- Nishii, A
- Kikuchi, T
- Mori, T
- Shimura, N
- Sasaki, G
- Kizu, R
- Takubo, N
- Soneda, S
- Fujisawa, T
- Takaya, R
- Kizaki, Z
- Kanzaki, S
- Hanaki, K
- Matsuura, N
- Kasahara, Y
- Kosaka, K
- Takahashi, T
- Minamitani, K
- Matsuo, S
- Mochizuki, H
- Kobayashi, K
- Koike, A
- Horikawa, R
- Teno, S
- Tsubouchi, K
- Mochizuki, T
- Igarashi, Y
- Amemiya, S
- Sugihara, S
Producer: 20180213
In:
Diabetic medicine : a journal of the British Diabetic Association vol. 34
Availability: No items available.
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