These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
161 related articles for article (PubMed ID: 756394)
21. Familial D-D translocation. A family showing transmission through three generations; a case with multiple congenital malformations, and a case of regular 21-trisomic Down's syndrome. Visfeldt J Acta Pathol Microbiol Scand; 1969; 75(4):545-54. PubMed ID: 4246134 [No Abstract] [Full Text] [Related]
22. [MULTIPLE CONGENITAL MALFORMATIONS ASSOCIATED TO A DOUBLE CHROMOSOMAL ANOMALY: TRIPLE-X AND 17-18 TRISOMY]. RICCI N; CASTOLDI GL; BORGATTI L; ALBERTI R Acta Genet Med Gemellol (Roma); 1964 Jul; 13():253-65. PubMed ID: 14198923 [No Abstract] [Full Text] [Related]
23. [Comparative pathology of trisomies D and E]. Bocquet L Union Med Can; 1968 Jul; 97(7):907-23. PubMed ID: 5709533 [No Abstract] [Full Text] [Related]
24. [Application of single nucleotide polymorphism array in prenatal diagnosis for fetuses with abnormal ultrasound findings]. Guo YL; Wang L; Xue SW; Qu SZ; Yang J; Xu H; Bai ZX; Liu N; Kong XD Zhonghua Fu Chan Ke Za Zhi; 2018 Jul; 53(7):464-470. PubMed ID: 30078256 [No Abstract] [Full Text] [Related]
25. [Genetic aspects of teratology]. Laziuk GI; Lur'e IV Vestn Akad Med Nauk SSSR; 1982; (6):24-32. PubMed ID: 7051613 [No Abstract] [Full Text] [Related]
26. [Hereditary factors and their causative role in anatomic variation]. Usoev SS; Shved IA Arkh Anat Gistol Embriol; 1986 Jan; 90(1):16-22. PubMed ID: 2937392 [TBL] [Abstract][Full Text] [Related]
28. Chromosomal survey in 298 normal subjects and 1,253 cases of congenital disorders during 1966-1970. Battaglia E; Guanti G; Barsanti P; Petrinelli P Acta Genet Med Gemellol (Roma); 1971 Apr; 20(2):123-73. PubMed ID: 4255243 [No Abstract] [Full Text] [Related]
29. Recognizable patterns of human malformation. Smith DW Major Probl Clin Pediatr; 1976; 7():1-497. PubMed ID: 940360 [No Abstract] [Full Text] [Related]
32. Use of fluorescent in situ hybridization to detect trisomy 13 in archival tissues for cytogenetic diagnosis. Drut RM; Harris CP; Drut R; Meisner L Pediatr Pathol; 1992; 12(6):799-805. PubMed ID: 1448389 [TBL] [Abstract][Full Text] [Related]
33. [Importance of the diagnosis of congenital developmental defects in the practice of pathologists]. Laziuk GI Arkh Patol; 1980; 42(7):24-8. PubMed ID: 7417019 [TBL] [Abstract][Full Text] [Related]
34. Diagnosis of genetic defects by chromosomal analysis. Ghani F; Maniar S; Khilji Z; Azim M; Khurshid M J Pak Med Assoc; 1995 Nov; 45(11):295-6. PubMed ID: 8920609 [TBL] [Abstract][Full Text] [Related]
35. Dysmorphology and short stature. Parkin JM Br Med Bull; 1981 Sep; 37(3):297-302. PubMed ID: 7034855 [No Abstract] [Full Text] [Related]