黒木, 良和, 1937-
黒木良和
Kuroki, Yoshikazu
黒木, 良和
VIAF ID: 25957780 (Personal)
Permalink: http://viaf.org/viaf/25957780
Preferred Forms
- 100 1 _ ‡a Kuroki, Yoshikazu
- 100 1 _ ‡a 黒木, 良和
- 100 1 _ ‡a 黒木, 良和 ‡d 1937-
- 100 1 _ ‡a 黒木, 良和, ‡d 1937-
- 100 0 _ ‡a 黒木良和
4xx's: Alternate Name Forms (8)
Works
Title | Sources |
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Brain MRI findings of older patients with Pallister-Killian syndrome | |
Ehlers-Danlos syndrome, vascular type: a novel missense mutation in the COL3A1 gene | |
Epilepsy and neurological findings in 11 individuals with 1p36 deletion syndrome | |
Favorable seizure outcome in Kabuki make-up syndrome associated with epilepsy | |
HRAS mutants identified in Costello syndrome patients can induce cellular senescence: possible implications for the pathogenesis of Costello syndrome | |
Magnetic resonance imaging abnormalities of the brain in Goldberg-Shprintzen syndrome (Hirschsprung disease, microcephaly, and iris coloboma) | |
No sex differences in 18 trisomy births in the Kanagawa Birth Defects Monitoring Program | |
On the Ring 13 Chromosome in a Malformed Infant with Special Regard to the Break Point | |
Paternal UPD14 is responsible for a distinctive malformation complex | |
Premature thelarche in Rubinstein-Taybi syndrome | |
Seishin chitai no igaku to kyōiku, 1982 (a.e.) | |
Shin senten kikei shokogun atorasu. | |
Sotos syndrome associated with a de novo balanced reciprocal translocation t(5;8)(q35;q24.1). | |
Trends in occurrence of twin births in Japan | |
Update of the genotype and phenotype of KMT2D and KDM6A by genetic screening of 100 patients with clinically suspected Kabuki syndrome | |
Zusetsu senshokutai ijō | |
ダウン症候群 | |
図說染色体異常 | |
新先天奇形症候群アトラス = New Atlas of Congenital Malformation Syndromes | |
精神遅滞の医学と教育 |