Results 121 to 130 of about 12,301 (210)

First Case Report of Agnathia-Otocephaly Complex Reported in Niger. [PDF]

Clin Case Rep
Diaouga HS, Dogbe YZKO, Garba RM, Nayama M.   +3 more
europepmc   +1 more source

Antenatal discovery of mosaic trisomy 14 in an early-onset malformative syndrome. [PDF]

Mol Cytogenet
Martineau R, Fuchs F, Lamouroux A, Ganne B, Wells C.   +4 more
europepmc   +1 more source

Antenatal ultrasound diagnosis of fetal micrognathia: validation and reproducibility of quantitative methods. [PDF]

Ultrasound Obstet Gynecol
Denk MC, Bertin M, Donadono V, Kangesu L, Yulia A, Ushakov F, Pandya PP, Napolitano R.   +7 more
europepmc   +1 more source

Clinical Feasibility and Surgical Outcomes of a 3D-Printed Template-Based PMMA Implant Workflow for Genioplasty. [PDF]

J Clin Med
Kim S, Yun YM, Ha C, Kang DH, Park S.
europepmc   +1 more source

Pycnodysostosis Revealed by Recurrent Fractures: Report of Two Cases. [PDF]

Cureus
Hamoutahra A, Talha H.
europepmc   +1 more source

<i>SRSF1</i> haploinsufficiency drives the neurodevelopmental phenotype of the 17q22 deletion syndrome. [PDF]

Front Med (Lausanne)
Wu Y, Gao C, Chen Z, Liu F, Yuan J, Cheng W.   +5 more
europepmc   +1 more source

Hallermann-Streiff syndrome: A systematic review of the published literature. [PDF]

J Oral Biol Craniofac Res
Abbas R, Krishna R, Garg A.
europepmc   +1 more source

Phenocopies of 22q11.2DS: revealing genetic diversity in clinically suspected 22q11.2 deletion syndrome. [PDF]

Mol Cell Pediatr
Szumutku F, Lengyel A, Pinti É, Kun I, Németh K, Abonyi T, Gál F, Ryu SW, Song Y, Ujfalusi A, Kádár K, Jávorszky E, Tory K, Kis É, Goda V, Kriván G, Kovács ÁF, Haltrich I.   +17 more
europepmc   +1 more source

Perioperative Care of a Four-Year-Old Child With Teebi Hypertelorism Syndrome: A Rare Craniofacial Disorder. [PDF]

J Med Cases
Abdelhady E, Tobias JD.
europepmc   +1 more source