Jones KL - Search Results

1

FG syndrome, an X-linked multiple congenital anomaly syndrome: the clinical phenotype and an algorithm for diagnostic testing.

Clark RD, Graham JM Jr, Friez MJ, Hoo JJ, Jones KL, McKeown C, Moeschler JB, Raymond FL, Rogers RC, Schwartz CE, Battaglia A, Lyons MJ, Stevenson RE. Clark RD, et al. Among authors: jones kl. Genet Med. 2009 Nov;11(11):769-75. doi: 10.1097/GIM.0b013e3181bd3d90. Genet Med. 2009. PMID: 19938245 Free PMC article.

2

Morphogenesis: Re: Clinical, natural history, and imaging information on patients included in reports.

Aylsworth A, Graham JM Jr, Hall JG, Hoyme HE, Jones KL, Stevenson RE. Aylsworth A, et al. Among authors: jones kl. Am J Med Genet A. 2003 May 15;119A(1):93; discussion 94. doi: 10.1002/ajmg.a.10185. Am J Med Genet A. 2003. PMID: 12707969 No abstract available.

3

Contribution of clinical teratologists and geneticists to the evaluation of the etiology of congenital malformations alleged to be caused by environmental agents: ionizing radiation, electromagnetic fields, microwaves, radionuclides, and ultrasound.

Graham JM Jr, Jones KL, Brent RL. Graham JM Jr, et al. Among authors: jones kl. Teratology. 1999 Apr;59(4):307-13. doi: 10.1002/(SICI)1096-9926(199904)59:4<307::AID-TERA18>3.0.CO;2-O. Teratology. 1999. PMID: 10331535

4

Chromosome 10qter deletion syndrome: a review and report of three new cases.

Wulfsberg EA, Weaver RP, Cunniff CM, Jones MC, Jones KL. Wulfsberg EA, et al. Among authors: jones kl, jones mc. Am J Med Genet. 1989 Mar;32(3):364-7. doi: 10.1002/ajmg.1320320319. Am J Med Genet. 1989. PMID: 2658586 Review.

5

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

Kosaki K, Curry CJ, Roeder E, Jones KL. Kosaki K, et al. Among authors: jones kl. 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.

6

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

Jones KL, Kosaki K, Hall BD. Jones KL, et al. 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

7

X-linked laterality sequence: situs inversus, complex cardiac defects, splenic defects.

Mathias RS, Lacro RV, Jones KL. Mathias RS, et al. Among authors: jones kl. Am J Med Genet. 1987 Sep;28(1):111-6. doi: 10.1002/ajmg.1320280116. Am J Med Genet. 1987. PMID: 3674105

8

Laterality defects in conjoined twins: implications for normal asymmetry in human embryogenesis.

Cunniff C, Jones KL, Jones MC, Saunders B, Shepard T, Benirschke K. Cunniff C, et al. Among authors: jones kl, jones mc. Am J Med Genet. 1988 Nov;31(3):669-77. doi: 10.1002/ajmg.1320310323. Am J Med Genet. 1988. PMID: 3228146

9

Autosomal dominant benign neonatal seizures.

Cunniff C, Wiedlin N, Jones KL. Cunniff C, et al. Among authors: jones kl. Am J Med Genet. 1988 Aug;30(4):963-6. doi: 10.1002/ajmg.1320300414. Am J Med Genet. 1988. PMID: 3189416

10

Delineation of the Costello syndrome.

Martin RA, Jones KL. Martin RA, et al. Among authors: jones kl. Am J Med Genet. 1991 Dec 1;41(3):346-9. doi: 10.1002/ajmg.1320410316. Am J Med Genet. 1991. PMID: 1789291

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