TY  - GEN
AU  - Derrien,C
AU  - Odent,S
AU  - Henry,C
AU  - De La Villemarque,R
AU  - Poirier,J Y
AU  - Maugendre,D
TI  - [Pseudohypoparathyroidism or hypoparathyroidism? A misleading clinical presentation]
SN  - 0003-4266
PY  - 2002///0329
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Adult
KW  - Chromosome Deletion
KW  - Chromosome Disorders
KW  - diagnosis
KW  - Chromosomes, Human, Pair 22
KW  - ultrastructure
KW  - Diagnosis, Differential
KW  - Face
KW  - abnormalities
KW  - Female
KW  - Fibrous Dysplasia, Polyostotic
KW  - Humans
KW  - Hypercalcemia
KW  - congenital
KW  - Hypoparathyroidism
KW  - In Situ Hybridization, Fluorescence
KW  - Infant, Newborn
KW  - Intellectual Disability
KW  - etiology
KW  - Obesity
KW  - Parathyroid Hormone
KW  - deficiency
KW  - Phenotype
KW  - Phosphorus
KW  - blood
KW  - Pregnancy
KW  - Pregnancy Complications
KW  - Pseudohypoparathyroidism
KW  - Purpura, Thrombocytopenic, Idiopathic
KW  - complications
KW  - Scoliosis
KW  - Syndrome
KW  - Velopharyngeal Insufficiency
N1  - Publication Type: Case Reports; English Abstract; Journal Article
ER  -