Pia Hermanns und Joachim Pohlenz - Info zur Person

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A new heterozygous mutation (D196N) in the Gs alpha gene as a ...www.degruyter.com › document › doi › jpem › pdf

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Julia Winter 1, Olaf Hiort 2, Pia Hermanns 1,. Susanne Thiele 2 and Joachim Pohlenz 1,*. 1 Children ' s Hospital of the Johannes Gutenberg-University ,.

European Journal of Medical Genetics | Vol 60, Issue 5, Pages www.sciencedirect.com › journal › vol › issue

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Mira Kharbanda, Pia Hermanns, Jeremy Jones, Joachim Pohlenz, ... Malcolm Donaldson. Pages : Download PDF. Article preview.

A novel deletion in the thyrotropin Beta-subunit gene PubMedpubmed.ncbi.nlm.nih.gov › ...

pubmed.ncbi.nlm.nih.gov

Authors. Pia Hermanns , Robert Couch, Norma Leonard, Cherise Klotz, Joachim Pohlenz. Affiliation. 1 Department of Pediatrics, Johannes Gutenberg University ...

Determination of thyroid volume in infants with suspected congenital ...www.birpublications.org › doi › abs › bjro

www.birpublications.org

· Chourouk Mansour,; Yasmine Ouarezki,; Jeremy Huw Jones,; Morag Green,; Emily Jane Stenhouse,; Greg Irwin,; Pia Hermanns,; Joachim Pohlenz ...

Novel heterozygous thyrotropin receptor mutation presenting with ...pubmed.ncbi.nlm.nih.gov › ...

pubmed.ncbi.nlm.nih.gov

Authors. Angela Lucas-Herald , Therese Bradley, Pia Hermanns, Jeremy Jones, Morag Attaie, Elaine Thompson, Joachim Pohlenz, Malcolm Donaldson ...

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Sophie Stoppa-Vaucher, MD, Diane Francoeur, MD, Andrée Grignon, MD, Nathalie Alos, MD, Joachim Pohlenz, MD, Pia Hermanns, MD, Guy Van Vliet, MD, ...

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