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22. Turner phenotype: mosaic 45,X-47,XY, plus 18. Schinzel A; Schmid W; Prader A J Med Genet; 1974 Mar; 11(1):101-4. PubMed ID: 4135076 [TBL] [Abstract][Full Text] [Related]
23. [Two sisters with major gonadal dysgenesis, dwarfism, microcephaly, arachnodactyly, and normal karyotype 46, XX]. Maximilian C; Ionescu B; Bucur A J Genet Hum; 1970 Dec; 18(4):365-78. PubMed ID: 5524817 [No Abstract] [Full Text] [Related]
24. [Cutis verticis gyrata in a newborn infant]. Hernández Rastrollo R; Martínez Tallo E; Galan Gómez E; Cardesa García JJ An Esp Pediatr; 1993 Nov; 39(5):466-7. PubMed ID: 8285472 [No Abstract] [Full Text] [Related]
25. [The role of genetic factors in the etiology of anomalies of permanent tooth root]. Beliakov IuA; Aubov AA; Titov VI Stomatologiia (Mosk); 1974; 53(6):54-7. PubMed ID: 4531753 [No Abstract] [Full Text] [Related]
26. Turner syndrome: the Leuven experience (1965-1989) in 478 patients. I. Patient's age at the time of diagnosis in relation to chromosomal findings. Kleczkowska A; Kubien E; Fryns JP; Van den Berghe H Genet Couns; 1990; 1(3-4):235-40. PubMed ID: 2098047 [TBL] [Abstract][Full Text] [Related]
27. Trisomy 4p in a family with A t(4;15). Hustinx WJ; Gabreëls JM; Kirkels VG; Korten JJ; Scheres JM; Joosten EM; Rutten FJ Ann Genet; 1975 Mar; 18(1):13-9. PubMed ID: 1080034 [TBL] [Abstract][Full Text] [Related]
29. Autosomal/heterosomal mixoploids: a report on two patients, a female with a 45, Z/47,XX plus 21 and a male with A 45,X/47,XY, plus 21 chromosome constitution. Hustinx TW; Haar BG; Scheres JM; Rutten FJ Ann Genet; 1974 Dec; 17(4):225-34. PubMed ID: 4281287 [No Abstract] [Full Text] [Related]
30. Ambiguous genitalia in neonates: a 4-year prospective study in a localized area. Al-Mulhim AN; Kamal HM East Mediterr Health J; 2010 Feb; 16(2):214-7. PubMed ID: 20799577 [TBL] [Abstract][Full Text] [Related]