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.
122 related articles for article (PubMed ID: 2376858)
1. Construction of a family pedigree in genetic counseling before amniocentesis. Langer A; Kudart E J Reprod Med; 1990 Jul; 35(7):715-8. PubMed ID: 2376858 [TBL] [Abstract][Full Text] [Related]
2. The importance of genetic counseling before amniocentesis. Cohn GM; Gould M; Miller RC; Habecker-Green J; Macri CJ; Gimovsky ML J Perinatol; 1996; 16(5):352-7; quiz 358-9. PubMed ID: 8915933 [TBL] [Abstract][Full Text] [Related]
3. Genetic counseling before prenatal diagnosis for advanced maternal age: an important medical safeguard. Rubin SP; Malin J; Maidman J Obstet Gynecol; 1983 Aug; 62(2):155-9. PubMed ID: 6866356 [TBL] [Abstract][Full Text] [Related]
4. The impact of first-trimester screening on AMA patients' uptake of invasive testing. Wray AM; Ghidini A; Alvis C; Hodor J; Landy HJ; Poggi SH Prenat Diagn; 2005 May; 25(5):350-3. PubMed ID: 15906421 [TBL] [Abstract][Full Text] [Related]
5. Impact of genetic counseling on primary and preventive care in obstetrics and gynecology. Cohn GM; Miller RC; Gould M; Macri CJ; Gimovsky ML J Reprod Med; 1999 Jan; 44(1):7-10. PubMed ID: 9987732 [TBL] [Abstract][Full Text] [Related]
6. The usefulness of a prenatal genetic questionnaire in genetic risk assessment. Cohn GM; Cimaroli T; Gould M; Macri CJ; Habecker-Green J; Miller RC Obstet Gynecol; 1996 Nov; 88(5):806-10. PubMed ID: 8885918 [TBL] [Abstract][Full Text] [Related]
7. Fetal oculocerebrorenal syndrome of Lowe associated with elevated maternal serum and amniotic fluid alpha-fetoprotein levels. Miller RC; Wolf EJ; Gould M; Macri CJ; Charnas LR Obstet Gynecol; 1994 Jul; 84(1):77-80. PubMed ID: 7516514 [TBL] [Abstract][Full Text] [Related]
8. Encouraging patients to undergo prenatal genetic counseling before the day of amniocentesis. Its effect on the use of amniocentesis. Lorenz RP; Botti JJ; Schmidt CM; Ladda RL J Reprod Med; 1985 Dec; 30(12):933-5. PubMed ID: 3908677 [TBL] [Abstract][Full Text] [Related]
10. Psychological aspects of genetic counseling: analysis of a transcript. Kessler S Am J Med Genet; 1981; 8(2):137-53. PubMed ID: 7282769 [TBL] [Abstract][Full Text] [Related]
11. Impact of genetic counseling and prenatal diagnosis for Down syndrome and neural tube defects. Swerts A Birth Defects Orig Artic Ser; 1987; 23(2):61-83. PubMed ID: 2954594 [TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of congenital myotonic dystrophy and counseling of the pregnant mother: case report and literature review. Geifman-Holtzman O; Fay K Am J Med Genet; 1998 Jul; 78(3):250-3. PubMed ID: 9677060 [TBL] [Abstract][Full Text] [Related]
13. [The problem of sex chromosome aneuploidy in genetic counseling using amniocentesis]. Engel E; Engel-De Montmollin M; Delozier C J Genet Hum; 1980 Sep; 28(3):257-66. PubMed ID: 7463026 [TBL] [Abstract][Full Text] [Related]
14. Who should be tested for fragile X carriership? A review of 1 center's pedigrees. Rajendra K; Bringman JJ; Ward J; Phillips OP Am J Obstet Gynecol; 2008 May; 198(5):e51-3. PubMed ID: 18358452 [TBL] [Abstract][Full Text] [Related]
15. The relevance of pre-amniocentesis pedigree analysis and genetic counseling. Holzgreve B; Holzgreve W; Golbus MS Clin Genet; 1983 Dec; 24(6):429-33. PubMed ID: 6652956 [TBL] [Abstract][Full Text] [Related]
16. [Genetic counseling and prenatal diagnosis in families with neural tube defects]. Mikiel-Kostyra K Probl Med Wieku Rozwoj; 1983; 12():244-62. PubMed ID: 6674977 [TBL] [Abstract][Full Text] [Related]
18. Anxiety and prenatal testing: do women with soft ultrasound findings have increased anxiety compared to women with other indications for testing? Hoskovec J; Mastrobattista JM; Johnston D; Kerrigan A; Robbins-Furman P; Wicklund CA Prenat Diagn; 2008 Feb; 28(2):135-40. PubMed ID: 18236427 [TBL] [Abstract][Full Text] [Related]
19. Prenatal molecular diagnosis of oculocutaneous albinism (OCA) in a large cohort of Israeli families. Rosenmann A; Bejarano-Achache I; Eli D; Maftsir G; Mizrahi-Meissonnier L; Blumenfeld A Prenat Diagn; 2009 Oct; 29(10):939-46. PubMed ID: 19626598 [TBL] [Abstract][Full Text] [Related]
20. Taking the family history in genetic disease: a guide for ophthalmologists. Stroh E Curr Opin Ophthalmol; 2011 Sep; 22(5):340-6. PubMed ID: 21730845 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]