@article {Wellington:August 1999:0009-9163:110,
	author = "Wellington, Cheryl",
	author = "Hackam, Abigail S.",
	title = "HotSpots - Insufficient death: autoimmune lymphoproliferative syndrome",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "110-111(2)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00001"
	doi = "doi:10.1034/j.1399-0004.1999.560202.x"
}

@article {Wellington:August 1999:0009-9163:112,
	author = "Wellington, Cheryl",
	author = "Hackam, Abigail S.",
	title = "HotSpots - Cutting it close: new insights into presenilin-1 function",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "112-113(2)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00002"
	doi = "doi:10.1034/j.1399-0004.1999.5602021.x"
}

@article {Wellington:August 1999:0009-9163:113,
	author = "Wellington, Cheryl",
	author = "Hackam, Abigail S.",
	title = "HotSpots - An unusual ataxia",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "113-115(3)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00003"
	doi = "doi:10.1034/j.1399-0004.1999.5602022.x"
}

@article {Mhanni:August 1999:0009-9163:116,
	author = "Mhanni, Aizeddin A",
	author = "Chudley, Albert E",
	title = "Genetic landmarks through philately Kabuki theater and Kabuki syndrome",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "116-117(2)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00004"
	doi = "doi:10.1034/j.1399-0004.1999.560203.x"
}

@article {Sadovnick:August 1999:0009-9163:118,
	author = "Sadovnick, AD",
	author = "Dircks, A",
	author = "Ebers, GC",
	title = "Genetic counselling in multiple sclerosis: risks to sibs and children of affected individuals",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "118-122(5)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00005"
	doi = "doi:10.1034/j.1399-0004.1999.560204.x"
}

@article {Heilstedt:August 1999:0009-9163:123,
	author = "Heilstedt, HA",
	author = "Shapira, SK",
	author = "Gregg, AR",
	author = "Shaffer, LG",
	title = "Molecular and clinical characterization of a patient with duplication of 1p36.3 and metopic synostosis",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "123-128(6)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00006"
	doi = "doi:10.1034/j.1399-0004.1999.560205.x"
}

@article {Durak:August 1999:0009-9163:129,
	author = "Durak, Beyhan",
	author = "Hakan Ozon, Yavuz",
	author = "Ozdemir, Muhsin",
	author = "Artan, Sevilhan",
	author = "Basaran, Nurettin",
	author = "Basaran, Seher",
	author = "Ozkinay, Cihangir",
	title = "FISH analysis with locus-specific probes in sperm from two translocation carrier men",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "129-135(7)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00007"
	doi = "doi:10.1034/j.1399-0004.1999.560206.x"
}

@article {Jiang:August 1999:0009-9163:136,
	author = "Jiang, Cao-Yang",
	author = "Esufali, Susmita",
	author = "Berk, Terri",
	author = "Gallinger, Steven",
	author = "Cohen, Zane",
	author = "Tobi, Martin",
	author = "Redston, Mark",
	author = "Bapat, Bharati",
	title = "STK11/LKB1 germline mutations are not identified in most PeutzJeghers syndrome patients",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "136-141(6)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00008"
	doi = "doi:10.1034/j.1399-0004.1999.560207.x"
}

@article {Speer:August 1999:0009-9163:142,
	author = "Speer, MC",
	author = "Nye, J",
	author = "McLone, D",
	author = "Worley, G",
	author = "Melvin, EC",
	author = "Viles, KD",
	author = "Franklin, A",
	author = "Drake, C",
	author = "Mackey, J",
	author = "George, TM",
	title = "Possible interaction of genotypes at cystathionine -synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "142-144(3)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00009"
	doi = "doi:10.1034/j.1399-0004.1999.560208.x"
}

@article {Sarafoglou:August 1999:0009-9163:145,
	author = "Sarafoglou, Kyriake",
	author = "Funai, Edmund F",
	author = "Fefferman, Nancy",
	author = "Zajac, Laura",
	author = "Geneiser, Nancy",
	author = "Paidas, Michael J",
	author = "Greco, Alba",
	author = "Wallerstein, Robert",
	title = "Short rib-polydactyly syndrome: more evidence of a continuous spectrum",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "145-148(4)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00010"
	doi = "doi:10.1034/j.1399-0004.1999.560209.x"
}

@article {Faure:August 1999:0009-9163:149,
	author = "Faure, Sabine",
	author = "Bordelais, Isabelle",
	author = "Marquette, Catherine",
	author = "Rittey, Chris",
	author = "Campos-Castello, Jaime",
	author = "Goutieres, Francoise",
	author = "Ponsot, Gerard",
	author = "Weissenbach, Jean",
	author = "Lebon, Pierre",
	title = "AicardiGoutieres syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "149-153(5)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00011"
	doi = "doi:10.1034/j.1399-0004.1999.560210.x"
}

@article {Mhanni:August 1999:0009-9163:154,
	author = "Mhanni, AA",
	author = "Cross, HG",
	author = "Chudley, AE",
	title = "Kabuki syndrome: description of dental findings in 8 patients",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "154-157(4)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00012"
	doi = "doi:10.1034/j.1399-0004.1999.560211.x"
}

@article {Boer:August 1999:0009-9163:158,
	author = "Boer, Jolanda MA",
	author = "Kuivenhoven, Jan Albert",
	author = "Feskens, Edith JM",
	author = "Schouten, Evert G",
	author = "Havekes, Louis M",
	author = "Seidell, Jacob C",
	author = "Kastelein, John JP",
	author = "Kromhout, Daan",
	title = "Physical activity modulates the effect of a lipoprotein lipase mutation (D9N) on plasma lipids and lipoproteins",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "158-163(6)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00013"
	doi = "doi:10.1034/j.1399-0004.1999.560212.x"
}

@article {:August 1999:0009-9163:164,
	title = "Serum total IgE levels and CD14 on chromosome 5q31",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "164-165(2)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00014"
	doi = "doi:10.1034/j.1399-0004.1999.560213.x"
}

@article {:August 1999:0009-9163:166,
	title = "Association between CAG repeat number in the androgen receptor and male infertility in a Belgian study",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "166-167(2)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00015"
	doi = "doi:10.1034/j.1399-0004.1999.560214.x"
}

@article {:August 1999:0009-9163:168,
	title = "High frequency of type 1 GM1 gangliosidosis in southern Brazil",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "168-169(2)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00016"
	doi = "doi:10.1034/j.1399-0004.1999.560215.x"
}

@article {:August 1999:0009-9163:170,
	title = "Scalp-ear-nipple (FinlayMarks) syndrome: a familial case with renal involvement",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "170-172(3)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00017"
	doi = "doi:10.1034/j.1399-0004.1999.560216.x"
}

@article {:August 1999:0009-9163:173,
	title = "A Japanese patient homozygous for the H1085R mutation in the CFTR gene presents with a severe form of cystic fibrosis",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "173-175(3)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00018"
	doi = "doi:10.1034/j.1399-0004.1999.560217.x"
}

@article {:August 1999:0009-9163:176,
	title = "Correspondence",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "176-176(1)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00019"
	doi = "doi:10.1034/j.1399-0004.1999.560218.x"
}

@article {Author:August 1999:0009-9163:177,
	author = "Author, An",
	title = "Correspondence",
	journal = "Clinical Genetics",
	volume = "56",
	year = "August 1999",
	pages = "177-177(1)",
	url = {http://www.ingentaconnect.com/content/mksg/cge/1999/00000056/00000002/art00020"
	doi = "doi:10.1034/j.1399-0004.1999.560219.x"
}