Results 101 to 110 of about 5,413 (169)

(Epi)genotype-phenotype correlations of Beckwith-Wiedemann syndrome in China. [PDF]

Ital J Pediatr
Lan D, Zhang S, Li J, Wang Y, Dong C.
europepmc   +1 more source

Oral mucosal health in acromegaly: clinical insights and metabolic associations. [PDF]

BMC Oral Health
Cengiz BC, Polat SB, Yildizer E, Ates I, Ersoy R, Topaloglu O, Cakir B.   +6 more
europepmc   +1 more source

Clinical phenotype and molecular genetic analysis of 24 cases of Beckwith-Wiedemann syndrome. [PDF]

Transl Pediatr
Wu Z, Yin X, Li X, Mei H, Li J, Huang Z, Cheng J, Yi P, Zhang W, Xu A.   +9 more
europepmc   +1 more source

Case Report: Familial partial lipodystrophy, description of novel and ultrarare variants with distinct phenotypic spectrum. [PDF]

Front Endocrinol (Lausanne)
Magno S, Pelosini C, Paoli M, Gilio D, Palladino L, Menconi F, Barison A, Todiere G, Ortori S, Coco B, Paolucci G, Salvetti G, Sessa MR, Ceccarini G, Santini F.   +14 more
europepmc   +1 more source

Two Infants with Beckwith-Wiedemann Syndrome

Balkan Journal of Medical Genetics, 2010
Ratbi I, Elalaoui S, Sefiani A
doaj   +1 more source

Analysis on the plane and mechanism of tongue-originated obstruction in Obstructive Sleep Apnea Syndrome (OSAS) patients with macroglossia. [PDF]

Braz J Otorhinolaryngol
Huang M, Chen G.
europepmc   +1 more source

Rare Oral Manifestations of Systemic Amyloidosis: A Case Report. [PDF]

Case Rep Hematol
Barazanji S, Herrera JG, Garming-Legert K.   +2 more
europepmc   +1 more source

Cardiofaciocutaneous Syndrome Type 4 due to a MAP2K2 Variant: Expanding the Phenotypic Spectrum With Feeding Dysfunction and Neurodevelopmental Involvement. [PDF]

Clin Case Rep
Świeca A, Rydzanicz M, Ploski R, Szczałuba K.   +3 more
europepmc   +1 more source

Macroglossia.

Indian pediatrics, 2004
A K, Dubey, Kirandeep, Sodhi
openaire   +1 more source