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Binder phenotype and brachytelephalangic chondrodysplasia punctata secondary to maternal vitamin K deficiency
- Source :
- Clinical Dysmorphology, Clinical Dysmorphology, Lippincott, Williams & Wilkins, 2010, 19 (2), pp.85--87. ⟨10.1097/MCD.0b013e328335c14a⟩
- Publication Year :
- 2010
- Publisher :
- HAL CCSD, 2010.
-
Abstract
- International audience; no abstract
- Subjects :
- medicine.medical_specialty
Chondrodysplasia Punctata
[SDV]Life Sciences [q-bio]
Pathology and Forensic Medicine
03 medical and health sciences
Congenital
Young Adult
Pregnancy
Internal medicine
Vitamin K deficiency
Medicine
Humans
Chondrodysplasia punctata
Brachytelephalangic Chondrodysplasia Punctata
Child
Genetics (clinical)
ComputingMilieux_MISCELLANEOUS
030304 developmental biology
0303 health sciences
business.industry
030305 genetics & heredity
Infant, Newborn
Infant
General Medicine
Hand Deformities
medicine.disease
Newborn
Phenotype
3. Good health
Radiography
Pregnancy Complications
Endocrinology
K deficiency
Pediatrics, Perinatology and Child Health
Female
Vitamin K Deficiency
Anatomy
business
Hand Deformities, Congenital
Maternal vitamin
Subjects
Details
- Language :
- English
- ISSN :
- 09628827
- Database :
- OpenAIRE
- Journal :
- Clinical Dysmorphology, Clinical Dysmorphology, Lippincott, Williams & Wilkins, 2010, 19 (2), pp.85--87. ⟨10.1097/MCD.0b013e328335c14a⟩
- Accession number :
- edsair.doi.dedup.....77064c85ec7fbf951308b7628036c8ef