يعرض 1 - 6 نتائج من 6 نتيجة بحث عن '"Boehmer, ALM"', وقت الاستعلام: 0.33s تنقيح النتائج
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    Academic Journal
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    Academic Journal

    المصدر: Boehmer , ALM , Bruggenwirth , H , Van Assendelft , C , Otten , BJ , Verleun-Mooijman , MCT , Niermeijer , MF , Brunner , HG , Rouwe , CW , Waelkens , JJ , Oostdijk , W , Kleijer , WJ , Van der Kwast , TH , De Vroede , MA & Drop , SLS 2001 , ' Genotype versus phenotype in families with androgen insensitivity syndrome ' , Journal of Clinical Endocrinology and Metabolism , vol. 86 , no. 9 , pp. 4151-4160 .

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    Academic Journal

    المصدر: Boehmer , ALM , Brinkmann , AO , Sandkuijl , LA , Halley , DJJ , Niermeijer , MF , Andersson , S , de Jong , FH , Kayserili , H , de Vroede , MA , Otten , BJ , Rouwe , CW , Mendonca , BB , Rodrigues , C , Bode , HH , de Ruiter , PE , Delemarre-van de Waal , HA & Drop , SLS 1999 , ' 17 beta-hydroxysteroid dehydrogenase-3 deficiency : Diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations ' , Journal of Clinical ....

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    Academic Journal

    المساهمون: 124423

    Relation: JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM; Boehmer A., Brinkmann A., Sandkuijl L., Halley D., Niermeijer M., Andersson S., de Jong F., Kayserili H., de Vroede M., Otten B., et al., "17 beta-hydroxysteroid dehydrogenase-3 deficiency: Diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations", JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, cilt.84, ss.4713-4721, 1999; vv_1032021; av_d968a8cd-3799-4cb0-9e94-a4a27ae05cef; http://hdl.handle.net/20.500.12627/143404; https://doi.org/10.1210/jc.84.12.4713; 84; 12; 4713; 4721

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    Academic Journal

    المصدر: Current Opinion in Pulmonary Medicine; Jan2006, Vol. 12 Issue 1, p34-41, 8p