Results 231 to 240 of about 110,198 (324)

Genetic disorders and associated morbidity, mortality, and congenital anomalies in preterm infants born at less than 34 weeks of gestation. [PDF]

BMC Pediatr
Everett SS, Bomback M, Banerjee A, Sahni R, Wapner RJ, Tolia VN, Clark RH, Lyford A, Hays T.   +8 more
europepmc   +1 more source

Pilot evaluation of optical genome mapping in chronic lymphocytic leukemia: complementing FISH analysis. [PDF]

BMC Cancer
Erdem S, Bayrak Tokaç AG, Aday A, Karaca D, Mutlu MB, Çefle K, Yenerel MN, Öztürk Ş, Kalayoğlu Beşışık S.   +8 more
europepmc   +1 more source

DNA polymorphism analysis in families with recurrence of free trisomy 21

, 1992
Constantinos Pángalos, C. Conover Talbot, John G. Lewis, P A Adelsberger, Michael B. Petersen, Jean‐Louis Serre, M O Rethoré, Marie‐Christine de Blois, P. Parent, Albert Schinzel, Franz Binkert, Joëlle Boué, Elisabeth Corbin, M. F. Croquette, S Gilgenkrantz, J. de Grouchy, M. F. Bertheas, Marguerite Prieur, O Raoul, F Serville, Jean‐Pierre Siffroi, F. Thépot, J Lejeune, Stylianos E. Antonarakis   +23 more
openalex   +1 more source

The placental effects of trisomy for human chromosome 21 orthologs in four mouse models of Down syndrome. [PDF]

Biol Open
Sato T, Baxter LL, Adams AD, Bishop LA, Guedj F, Bianchi DW.   +5 more
europepmc   +1 more source

Low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with perinatal decrease of the trisomy 21 cell line, a favorable fetal outcome and a false negative second-trimester non-invasive prenatal testing result for down syndrome

Chih‐Ping Chen
openalex   +1 more source

Gene expression in and development of trisomies of Drosophila melanogaster

, 2010
Robert H. Devlin
openalex   +1 more source

Clinical Utility of Opportunistic Genome-Wide cfDNA Prenatal Screening in Intermediate-Risk Pregnancies. [PDF]

Genes (Basel)
Menao Guillén S, Pedrola L, Orellana C, Roselló M, Arruebo M, Lahuerta Pueyo C, Sobreviela Laserrada M, Marcos B, Pascual Mancho J, Cervera JV, Tajada M, Quiroga R.   +11 more
europepmc   +1 more source

Using the Fluorescence In Situ Hybridization in the Diagnosis of Trisomy 13 in a Male Newborn From Mali. [PDF]

Clin Case Rep
Maiga AB, Samassekou O, Sidibé CO, Traoré O, Maiga B, Traoré M, Guinto CO, Landouré G.   +7 more
europepmc   +1 more source

Persistent right umbilical vein in trisomy 18: sonographic observation.

, 1998
Luc De Catte, Kaan Osmanagaoglu, I De Schrijver   +2 more
openalex   +2 more sources