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Wachstumsstörungen als Leitsymptom

Wachstumsstörungen als Leitsymptom

http://www.wikidata.org/entity/Q57987126

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Wachstumsstörungen als Leitsymptom

http://www.wikidata.org/entity/Q57987126

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wetenschappelijk artikel

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наукова стаття, опублікована в червні 2012

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name

Wachstumsstörungen als Leitsymptom

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Wachstumsstörungen als Leitsymptom

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Wachstumsstörungen als Leitsymptom

@en

Wachstumsstörungen als Leitsymptom

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Wachstumsstörungen als Leitsymptom

@en

Wachstumsstörungen als Leitsymptom

@nl

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S11825-012-0331-2

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medizinische genetik

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Wachstumsstörungen als Leitsymptom

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A. Rauch

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P2860

GH therapy in Noonan syndrome: Review of final height data.

Evaluation of a district growth screening programme: the Oxford Growth Study.

Health supervision for children with achondroplasia.

Epigenotype-phenotype correlations in Silver-Russell syndrome

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia.

Growth and symptoms in Silver-Russell syndrome: review on the basis of 386 patients.

Genotypes and phenotypes in children with short stature: clinical indicators of SHOX haploinsufficiency

Enhancer deletions of the SHOX gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domain.

Enhancer elements upstream of the SHOX gene are active in the developing limb

ACMG practice guideline: genetic evaluation of short stature.

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s11825-012-0331-2

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123-137

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scholarly article

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10.1007/S11825-012-0331-2

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2

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24

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Christian T Thiel

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2012-06-01T00:00:00Z

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