• Issue

    Clinical Genetics: Volume 67, Issue 2

    107-191
    February 2005
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Mini Reviews

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Peroxisomal disorders I: biochemistry and genetics of peroxisome biogenesis disorders

RJA Wanders,  HR Waterham, 
  • Pages: 107-133
  • First Published: 24 November 2004
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The potential impact of genetic counseling for mental illness

JC Austin,  WG Honer, 
  • Pages: 134-142
  • First Published: 24 November 2004

Developmental Biology

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The developing limb and the control of the number of digits: Section Editor:
Jacques Michaud, e-mail: [email protected]

A Talamillo,  Mf Bastida,  M Fernandez-Teran,  Ma Ros, 
  • Pages: 143-153
  • First Published: 28 January 2005

HotSpots

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The vast array of opportunity for genomic discovery in human genetic disorders

ME Suzanne Lewis, 
  • Pages: 154-155
  • First Published: 28 January 2005
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Higher resolution solutions for mapping the mystery of idiopathic intellectual disability

  • Pages: 155-157
  • First Published: 28 January 2005
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A new frontier for fetal diagnosis using genomic CGH microarrays

  • Pages: 157-159
  • First Published: 28 January 2005

Original Article

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Genetic basis of hearing loss associated with enlarged vestibular aqueducts in Koreans

H-J Park,  S-J Lee,  H-S Jin,  JO Lee,  S-H Go,  HS Jang,  S-K Moon,  S-C Lee,  Y-M Chun,  H-K Lee,  J-Y Choi,  S-C Jung,  AJ Griffith,  SK Koo, 
  • Pages: 160-165
  • First Published: 20 December 2004

Short Reports

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Genetic susceptibility screening in schools: attitudes of the school community towards hereditary haemochromatosis

AA Gason,  MA Aitken,  SA Metcalfe,  KJ Allen,  MB Delatycki, 
  • Pages: 166-174
  • First Published: 07 December 2004
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Compound heterozygosity for two non-synonymous polymorphisms in NPC1L1 in a non-responder to ezetimibe

J Wang,  CM Williams,  RA Hegele, 
  • Pages: 175-177
  • First Published: 24 November 2004
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A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancer

E Lucci-Cordisco,  M Zollino,  S Baglioni,  I Mancuso,  R Lecce,  F Gurrieri,  A Crucitti,  L Papi,  G Neri,  M Genuardi, 
  • Pages: 178-182
  • First Published: 07 December 2004
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A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13

SHE Zaidi,  V Peltekova,  S Meyer,  A Lindinger,  AD Paterson,  L-C Tsui,  M Faiyaz-Ul-Haque,  AS Teebi, 
  • Pages: 183-188
  • First Published: 07 December 2004

Letter

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Multiplex ligation-dependent probe amplification is superior for detecting deletions/duplications in Duchenne muscular dystrophy

M Schwartz,  M Dunø, 
  • Pages: 189-191
  • First Published: 07 December 2004