Newborn with rhizomelia and difficulty breathing
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[1] S. Ferdinandusse,et al. Clinical and Biochemical Pitfalls in the Diagnosis of Peroxisomal Disorders , 2016, Neuropediatrics.
[2] A. Offiah,et al. Radiographic features of the skeleton in disorders of post-squalene cholesterol biosynthesis , 2015, Pediatric Radiology.
[3] N. Braverman,et al. Rhizomelic chrondrodysplasia punctata type 2 resulting from paternal isodisomy of chromosome 1 , 2010, American journal of medical genetics. Part A.
[4] E. Zackai,et al. Chondrodysplasia punctata associated with maternal autoimmune diseases: Expanding the spectrum from systemic lupus erythematosus (SLE) to mixed connective tissue disease (MCTD) and scleroderma report of eight cases , 2008, American journal of medical genetics. Part A.
[5] M. Irving,et al. Chondrodysplasia punctata: a clinical diagnostic and radiological review , 2008, Clinical dysmorphology.
[6] R. Lachman. Taybi and Lachman’s radiology of syndromes, metabolic disorders and skeletal dysplasias , 2006, La radiologia medica.
[7] R. Pauli,et al. Natural history of rhizomelic chondrodysplasia punctata , 2003, American journal of medical genetics. Part A.
[8] D. Wellesley,et al. Two cases of warfarin embryopathy: a re‐emergence of this condition? , 1998, British journal of obstetrics and gynaecology.