Results 191 to 200 of about 4,533 (250)

Malformation Pattern and Molecular Findings in the <i>FGFR1</i>-Related Hartsfield Syndrome Phenotype. [PDF]

Med Sci (Basel)
Gaudioso F, Pascolini G.
europepmc   +1 more source

Sparse Hair, Missing Teeth, Dry Skin: An Uncommon but Classic Condition.

Indian J Dermatol
Konda D, Reddy M.
europepmc   +1 more source

Idiopathic Harlequin Syndrome: A Case Report of an Uncommon Disease. [PDF]

Cureus
Singh M, Kumar Tyagi L.
europepmc   +1 more source

Nasal Myiasis in a Female with Christ-Siemens-Touraine Syndrome: A Case Report. [PDF]

JNMA J Nepal Med Assoc
Maharjan L, Shah A, Yadav D, Shrestha N.
europepmc   +1 more source

Kindler Syndrome in a 24-Year-Old Male: A Clinical Diagnosis in the Absence of Genetic Testing: A Rare Case Report. [PDF]

Case Rep Dermatol Med
Ahmad DS, Nasser R, Mahmoud A, Al-Janabi MH, Al-Shehabi Z, Hassan F.   +5 more
europepmc   +1 more source

Ectodermal dysplasia: a narrative review of the clinical and biological aspects relevant to oral health. [PDF]

Front Pediatr
Morandini AC, Adeogun O, Black M, Holman E, Collins K, James W, Lally L, Fordyce A, Dobbs R, McDaniel E, Putnam H, Milano M.   +11 more
europepmc   +1 more source