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1. Select result number 1
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   Clinical genetics

   published 1970

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2. Select result number 2
   2
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   Identification and functional analysis of novel mutations of the CLCNKB gene in Chinese patients with classic Bartter syndrome

   by Yu, Y, Xu, C, Pan, X, Ren, H, Wang, W, Meng, X, Huang, F, Chen, N
   Published in Clinical Genetics (2010)

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3. Select result number 3
   3
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   Map refinement of the Usher syndrome type 1B gene, MYO7A, relative to 11q13.5 microsatellite markers

   by Mouglabey, Yolla Bou, Nimri, Sawsan, Sayegh, Fouad, Zir, Elie El, Slim, Rima
   Published in Clinical Genetics (2008)

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4. Select result number 4
   4
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   Human Cytogenetic Nomenclature

   by Harnden, David
   Published in Clinical Genetics (2008)

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5. Select result number 5
   5
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   Three familial cases presenting with an immobile spine. Rigid spine or Emery-Dreifuss syndrome?

   by Spranger, M., Spranger, S., Ziegan, J., Lössner, J., Meinck, H.-M.
   Published in Clinical Genetics (2008)

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6. Select result number 6
   6
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   A complex rearrangement, including a deleted 8q, in a case of Langer-Giedion syndrome

   by Schwartz, S., Beisel, J. H., Panny, S. R., Cohen, M. M.
   Published in Clinical Genetics (2008)

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7. Select result number 7
   7
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   Marfan syndrome: a diagnostic dilemma

   by Viuoen, Denis, Beighton, Peter
   Published in Clinical Genetics (2008)

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8. Select result number 8
   8
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   Occurrence of sex chromosome mosaicism and translocation Down's syndrome in the same family

   by Smith, Arabella, Elliott, Gae
   Published in Clinical Genetics (2008)

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9. Select result number 9
   9
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   Next‐generation sequencing of Chinese stage IV lung cancer patients reveals an association between EGFR mutation status and survival outcome

   by Li, F., Du, X., Zhang, H., Ju, T., Chen, C., Qu, Q., Zhang, X., Qi, L., Lizée, G.
   Published in Clinical Genetics (2017)

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10. Select result number 10
    10
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    Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repair

    by Halley, D. J. J., Keijzer, W., Jaspers, N. G. J., Niermeuer, M. F., Rleijer, W. J., Boué, J., Boué, A., Bootsma, D.
    Published in Clinical Genetics (2008)

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11. Select result number 11
    11
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    From Ag phenotyping to molecular genetics: apolipoprotein B, serum lipid levels and coronary artery disease in Finland

    by Tikkanen, Matti J., Heliö, Tiina
    Published in Clinical Genetics (2008)

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12. Select result number 12
    12
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    At last - atlastin provides new insight into spastic paraplegia : HotSpots: HotSpots

    by Devon, RS
    Published in Clinical Genetics (2002)

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13. Select result number 13
    13
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    Low density lipoprotein receptor activity in cultured fibroblasts from subjects with or without ischemic heart disease (in the absence of familial hypercholesterolemia)*

    by Maartmann-Moe, Kjell, Magnus, Per, Børresen, Anne-Lise, Berg, Kare
    Published in Clinical Genetics (2008)

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14. Select result number 14
    14
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    Vascular ring leading to tracheoesophageal compression in a patient with Rubinstein-Taybi syndrome

    by Shashi, V., Fryburg, J. S.
    Published in Clinical Genetics (2008)

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15. Select result number 15
    15
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    A new autosomal dominant craniofacial deafness syndrome

    by Kassutto, S., Kassutto, Z., Ben-Ami, T., Goodman, R. M.
    Published in Clinical Genetics (2008)

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16. Select result number 16
    16
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    Familial occurrence of trophoblastic disease - report of recurrent molar pregnancies in sisters in three families

    by Ambani, L. M., Vaidya, R. A., Rao, C. S., Daftary, S. D., Motashaw, N. D.
    Published in Clinical Genetics (2008)

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17. Select result number 17
    17
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    A cystic fibrosis patient homozygous for 621 + 1G→T mutation has a severe pulmonary disease, mild pancreatic insufficiency and a gastro-esophageal reflux

    by Witt, Michal, Pogorzelski, Andrzej, Zebrak, Jerzy, Rutkiewicz, Ewa
    Published in Clinical Genetics (2008)

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18. Select result number 18
    18
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    Partial trisomy 2q

    by Schumacher, Robert E., Rocchini, Albert P., Wilson, Golder N.
    Published in Clinical Genetics (2008)

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19. Select result number 19
    19
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    Can we throw the master-switch in autoimmune disease? : HotSpots: HotSpots

    by Orban, Paul C, Levings, Megan K
    Published in Clinical Genetics (2003)

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20. Select result number 20
    20
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    Prenatal diagnosis of low level trisomy 15 mosaicism: review of the literature

    by Zaslav, AL, Fallet, S., Brown, S., Ebert, R., Fleischer, A., Valderama, E., Fox, JE
    Published in Clinical Genetics (2008)

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