@article {Sifakis:September 2001:0009-9163:165,
	author = "Sifakis, S",
	author = "Basel, D",
	author = "Ianakiev, P",
	author = "Kilpatrick, MW",
	author = "Tsipouras, P",
	title = "Distal limb malformations: underlying mechanisms and clinical associations",
	journal = "Clinical Genetics",
	volume = "60",
	year = "September 2001",
	pages = "165-172(8)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/2001/00000060/00000003/art00001"
	doi = "doi:10.1034/j.1399-0004.2001.600301.x"
}

@article {Warby:September 2001:0009-9163:173,
	author = "Warby, Simon",
	author = "Slow, Elizabeth",
	author = "Coburn, Bryan",
	title = "Discoveries in CharcotMarieTooth disease, Crohn's disease and BardetBiedl syndrome 4",
	journal = "Clinical Genetics",
	volume = "60",
	year = "September 2001",
	pages = "173-174(2)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/2001/00000060/00000003/art00002"
	doi = "doi:10.1034/j.1399-0004.2001.600302.1.x"
}

@article {Warby:September 2001:0009-9163:174,
	author = "Warby, Simon",
	author = "Slow, Elizabeth",
	author = "Coburn, Bryan",
	title = "Discoveries in CharcotMarieTooth disease, Crohn's disease and BardetBiedl syndrome 4",
	journal = "Clinical Genetics",
	volume = "60",
	year = "September 2001",
	pages = "174-176(3)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/2001/00000060/00000003/art00003"
	doi = "doi:10.1034/j.1399-0004.2001.600302.2.x"
}

@article {Warby:September 2001:0009-9163:176,
	author = "Warby, Simon",
	author = "Slow, Elizabeth",
	author = "Coburn, Bryan",
	title = "Discoveries in CharcotMarieTooth disease, Crohn's disease and BardetBiedl syndrome 4",
	journal = "Clinical Genetics",
	volume = "60",
	year = "September 2001",
	pages = "176-177(2)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/2001/00000060/00000003/art00004"
	doi = "doi:10.1034/j.1399-0004.2001.600302.3.x"
}

@article {Floros:September 2001:0009-9163:178,
	author = "Floros, J",
	author = "Fan, R",
	author = "Matthews, A",
	author = "DiAngelo, S",
	author = "Luo, J",
	author = "Nielsen, H",
	author = "Dunn, M",
	author = "Gewolb, I H",
	author = "Koppe, J",
	author = "van Sonderen, L",
	author = "Farri-Kostopoulos, L",
	author = "Tzaki, M",
	author = "Ramet, M",
	author = "Merrill, J",
	title = "Family-based transmission disequilibrium test (TDT) and casecontrol association studies reveal surfactant protein A (SP-A) susceptibility alleles for respiratory distress syndrome (RDS) and possible race differences",
	journal = "Clinical Genetics",
	volume = "60",
	year = "September 2001",
	pages = "178-187(10)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/2001/00000060/00000003/art00005"
	doi = "doi:10.1034/j.1399-0004.2001.600303.x"
}

@article {Kim:September 2001:0009-9163:188,
	author = "Kim, H",
	author = "Marcovina, SM",
	author = "Edwards, KL",
	author = "McKnight, B",
	author = "Bradley, CM",
	author = "McNeely, MJ",
	author = "Psaty, BM",
	author = "Motulsky, AG",
	author = "Austin, MA",
	title = "Lipoprotein(a) as a risk factor for maternal cardiovascular disease mortality in kindreds with familial combined hyperlipidemia or familial hypertriglyceridemia",
	journal = "Clinical Genetics",
	volume = "60",
	year = "September 2001",
	pages = "188-197(10)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/2001/00000060/00000003/art00006"
	doi = "doi:10.1034/j.1399-0004.2001.600304.x"
}

@article {Almqvist:September 2001:0009-9163:198,
	author = "Almqvist, EW",
	author = "Elterman, DS",
	author = "MacLeod, PM",
	author = "Hayden, MR",
	title = "High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British Columbia",
	journal = "Clinical Genetics",
	volume = "60",
	year = "September 2001",
	pages = "198-205(8)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/2001/00000060/00000003/art00007"
	doi = "doi:10.1034/j.1399-0004.2001.600305.x"
}

@article {Orellana:September 2001:0009-9163:206,
	author = "Orellana, C",
	author = "Martinez, F",
	author = "Badia, L",
	author = "Millan, JM",
	author = "Montero, MR",
	author = "Andres, J",
	author = "Prieto, F",
	title = "Trisomy rescue by postzygotic unbalanced (X;14) translocation in a girl with dysmorphic features",
	journal = "Clinical Genetics",
	volume = "60",
	year = "September 2001",
	pages = "206-211(6)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/2001/00000060/00000003/art00008"
	doi = "doi:10.1034/j.1399-0004.2001.600306.x"
}

@article {Joly:September 2001:0009-9163:212,
	author = "Joly, G",
	author = "Lapierre, J-M",
	author = "Ozilou, C",
	author = "Gosset, P",
	author = "Aurias, A",
	author = "de Blois, M-C",
	author = "Prieur, M",
	author = "Raoul, O",
	author = "Colleaux, L",
	author = "Munnich, A",
	author = "Romana, SP",
	author = "Vekemans, M",
	author = "Turleau, C",
	title = "Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype",
	journal = "Clinical Genetics",
	volume = "60",
	year = "September 2001",
	pages = "212-219(8)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/2001/00000060/00000003/art00009"
	doi = "doi:10.1034/j.1399-0004.2001.600307.x"
}

@article {Colomb:September 2001:0009-9163:220,
	author = "Colomb, E",
	author = "Nguyen, TD",
	author = "Bechetoille, A",
	author = "Dascotte, J-C",
	author = "Valtot, F",
	author = "Brezin, AP",
	author = "Berkani, M",
	author = "Copin, B",
	author = "Gomez, L",
	author = "Polansky, JR",
	author = "Garchon, H-J",
	title = "Association of a single nucleotide polymorphism in the TIGR/MYOCILIN gene promoter with the severity of primary open-angle glaucoma",
	journal = "Clinical Genetics",
	volume = "60",
	year = "September 2001",
	pages = "220-225(6)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/2001/00000060/00000003/art00010"
	doi = "doi:10.1034/j.1399-0004.2001.600308.x"
}

@article {Kotzot:September 2001:0009-9163:226,
	author = "Kotzot, D",
	title = "Comparative analysis of isodisomic and heterodisomic segments in cases with maternal uniparental disomy 14 suggests more than one imprinted region",
	journal = "Clinical Genetics",
	volume = "60",
	year = "September 2001",
	pages = "226-231(6)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/2001/00000060/00000003/art00011"
	doi = "doi:10.1034/j.1399-0004.2001.600309.x"
}

@article {Christian:September 2001:0009-9163:232,
	author = "Christian, SM",
	author = "Kieffer, SA",
	author = "Leonard, NJ",
	title = "Medical genetics and patient use of the Internet",
	journal = "Clinical Genetics",
	volume = "60",
	year = "September 2001",
	pages = "232-236(5)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/2001/00000060/00000003/art00012"
	doi = "doi:10.1034/j.1399-0004.2001.600310.x"
}

@article {Kamnasaran:September 2001:0009-9163:237,
	author = "Kamnasaran, D",
	author = "Gerritsen, JA",
	author = "McLeod, DR",
	author = "Cox, DW",
	title = "Features within the holoprosencephaly spectrum in sibs with a Robertsonian (14q;22q) translocation chromosome",
	journal = "Clinical Genetics",
	volume = "60",
	year = "September 2001",
	pages = "237-239(3)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/2001/00000060/00000003/art00013"
	doi = "doi:10.1034/j.1399-0004.2001.600311.x"
}

@article {Golfier:September 2001:0009-9163:240,
	author = "Golfier, Francois",
	author = "Peyrol, Simone",
	author = "Attia-Sobol, Jocelyne",
	author = "Marret, Henri",
	author = "Raudrant, Daniel",
	author = "Plauchu, Henri",
	title = "Hypermobility type of EhlersDanlos syndrome: influence of pregnancies",
	journal = "Clinical Genetics",
	volume = "60",
	year = "September 2001",
	pages = "240-241(2)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/2001/00000060/00000003/art00014"
	doi = "doi:10.1034/j.1399-0004.2001.600312.x"
}