Kosaki K - Search Results

1

Ritscher-Schinzel (3C) syndrome: documentation of the phenotype.

Kosaki K, Curry CJ, Roeder E, Jones KL. Kosaki K, et al. Am J Med Genet. 1997 Feb 11;68(4):421-7. doi: 10.1002/(sici)1096-8628(19970211)68:4<421::aid-ajmg10>3.0.co;2-u. Am J Med Genet. 1997. PMID: 9021015 Review.

2

Zimmer phocomelia: delineation by principal coordinate analysis.

Kosaki K, Jones MC, Stayboldt C. Kosaki K, et al. Am J Med Genet. 1996 Dec 2;66(1):55-9. doi: 10.1002/(SICI)1096-8628(19961202)66:1<55::AID-AJMG12>3.0.CO;2-P. Am J Med Genet. 1996. PMID: 8957512

3

Cervical flexion: its contribution to normal and abnormal cardiac morphogenesis.

Kosaki K, Mendoza A, Jones KL. Kosaki K, et al. Teratology. 1996 Sep;54(3):135-44. doi: 10.1002/(SICI)1096-9926(199609)54:3<135::AID-TERA3>3.0.CO;2-2. Teratology. 1996. PMID: 8987156

4

Parametric imaging of the chick embryonic cardiovascular system: a novel functional measure.

Kosaki K, Suzuki H, Schmid-Schönbein GW, Nelson TR, Jones KL. Kosaki K, et al. Pediatr Res. 1997 Apr;41(4 Pt 1):451-6. doi: 10.1203/00006450-199704000-00001. Pediatr Res. 1997. PMID: 9098844

5

Prader-Willi and Angelman syndromes: diagnosis with a bisulfite-treated methylation-specific PCR method.

Kosaki K, McGinniss MJ, Veraksa AN, McGinnis WJ, Jones KL. Kosaki K, et al. Am J Med Genet. 1997 Dec 19;73(3):308-13. Am J Med Genet. 1997. PMID: 9415690

6

Developmental delay in fetal aminopterin/methotrexate syndrome.

Del Campo M, Kosaki K, Bennett FC, Jones KL. Del Campo M, et al. Among authors: kosaki k. Teratology. 1999 Jul;60(1):10-2. doi: 10.1002/(SICI)1096-9926(199907)60:1<10::AID-TERA5>3.0.CO;2-H. Teratology. 1999. PMID: 10413333 Review.

7

Random X-inactivation in a girl with duplication Xp11.21-p21.3: report of a patient and review of the literature.

Matsuo M, Muroya K, Kosaki K, Ishii T, Fukushima Y, Anzo M, Ogata T. Matsuo M, et al. Among authors: kosaki k. Am J Med Genet. 1999 Sep 3;86(1):44-50. Am J Med Genet. 1999. PMID: 10440827 Review.

8

X-linked cubitus valgus with mental retardation and typical face.

Jones KL, Kosaki K, Hall BD. Jones KL, et al. Among authors: kosaki k. Am J Med Genet A. 2003 Nov 15;123A(1):33-6. doi: 10.1002/ajmg.a.20494. Am J Med Genet A. 2003. PMID: 14556244

9

Congenital hypothyroidism in Peters plus syndrome.

Kosaki R, Kamiishi A, Sugiyama R, Kawai M, Hasegawa T, Kosaki K. Kosaki R, et al. Among authors: kosaki k. Ophthalmic Genet. 2006 Jun;27(2):67-9. doi: 10.1080/13816810600678170. Ophthalmic Genet. 2006. PMID: 16754209

10

Umbilical cord length in urinary tract abnormalities associated with oligohydramnios: evidence regarding developmental pathogenesis.

Izumi K, Jones KL, Kosaki K, Benirschke K. Izumi K, et al. Among authors: kosaki k. Fetal Pediatr Pathol. 2006 Sep-Oct;25(5):233-40. doi: 10.1080/15513810601123326. Fetal Pediatr Pathol. 2006. PMID: 17438663

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