Fox M - Search Results

1

RAPADILINO syndrome: a multiple malformation syndrome with radial and patellar aplasia.

Jam K, Fox M, Crandall BF. Jam K, et al. Among authors: fox m. Teratology. 1999 Jul;60(1):37-8. doi: 10.1002/(SICI)1096-9926(199907)60:1<37::AID-TERA10>3.0.CO;2-R. Teratology. 1999. PMID: 10413338 No abstract available.

2

Attitudes toward genetic carrier screening for cystic fibrosis among pregnant women: the role of health beliefs and avoidant coping style.

Fang CY, Dunkel-Schetter C, Tatsugawa ZH, Fox MA, Bass HN, Crandall BF, Grody WW. Fang CY, et al. Among authors: fox ma. Womens Health. 1997 Spring;3(1):31-51. Womens Health. 1997. PMID: 9106369

3

PCR-based screening for cystic fibrosis carrier mutations in an ethnically diverse pregnant population.

Grody WW, Dunkel-Schetter C, Tatsugawa ZH, Fox MA, Fang CY, Cantor RM, Novak JM, Bass HN, Crandall BF. Grody WW, et al. Among authors: fox ma. Am J Hum Genet. 1997 Apr;60(4):935-47. Am J Hum Genet. 1997. PMID: 9106541 Free PMC article.

4

Radiographic and morphologic findings in a previously undescribed type of mesomelic dysplasia resembling atelosteogenesis type II.

Brodie SG, Lachman RS, Crandall BF, Fox MA, Rimoin DL, Cohn DH, Wilcox WR. Brodie SG, et al. Among authors: fox ma. Am J Med Genet. 1998 Nov 16;80(3):247-51. Am J Med Genet. 1998. PMID: 9843047

5

Education and testing strategy for large-scale cystic fibrosis carrier screening.

Tatsugawa ZH, Fox MA, Fang CY, Novak JM, Cantor RM, Bass HN, Dunkel-Schetter C, Crandall BF, Grody WW. Tatsugawa ZH, et al. Among authors: fox ma. J Genet Couns. 1994 Dec;3(4):279-89. doi: 10.1007/BF01412373. J Genet Couns. 1994. PMID: 24234134

6

Genetic testing as part of the early hearing detection and intervention (EHDI) process.

Schimmenti LA, Martinez A, Fox M, Crandall B, Shapiro N, Telatar M, Sininger Y, Grody WW, Palmer CG. Schimmenti LA, et al. Among authors: fox m. Genet Med. 2004 Nov-Dec;6(6):521-5. doi: 10.1097/01.gim.0000144187.21727.28. Genet Med. 2004. PMID: 15545749 Free article. No abstract available.

7

Infant hearing loss and connexin testing in a diverse population.

Schimmenti LA, Martinez A, Telatar M, Lai CH, Shapiro N, Fox M, Warman B, McCarra M, Crandall B, Sininger Y, Grody WW, Palmer CG. Schimmenti LA, et al. Among authors: fox m. Genet Med. 2008 Jul;10(7):517-24. doi: 10.1097/gim.0b013e31817708fa. Genet Med. 2008. PMID: 18580690

8

DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies.

Ji J, Lee H, Argiropoulos B, Dorrani N, Mann J, Martinez-Agosto JA, Gomez-Ospina N, Gallant N, Bernstein JA, Hudgins L, Slattery L, Isidor B, Le Caignec C, David A, Obersztyn E, Wiśniowiecka-Kowalnik B, Fox M, Deignan JL, Vilain E, Hendricks E, Horton Harr M, Noon SE, Jackson JR, Wilkens A, Mirzaa G, Salamon N, Abramson J, Zackai EH, Krantz I, Innes AM, Nelson SF, Grody WW, Quintero-Rivera F. Ji J, et al. Among authors: fox m. Eur J Hum Genet. 2015 Nov;23(11):1473-81. doi: 10.1038/ejhg.2015.71. Epub 2015 May 6. Eur J Hum Genet. 2015. PMID: 25944381 Free PMC article.

9

Why we do what we do: commentary on a reciprocal-engagement model of genetic counseling practice.

Fox M, Weil J, Resta R. Fox M, et al. J Genet Couns. 2007 Dec;16(6):729-30. doi: 10.1007/s10897-007-9118-z. Epub 2007 Oct 10. J Genet Couns. 2007. PMID: 17926124 No abstract available.

10

Ethnic differences in parental perceptions of genetic testing for deaf infants.

Palmer CG, Martinez A, Fox M, Sininger Y, Grody WW, Schimmenti LA. Palmer CG, et al. Among authors: fox m. J Genet Couns. 2008 Feb;17(1):129-38. doi: 10.1007/s10897-007-9134-z. Epub 2007 Oct 19. J Genet Couns. 2008. PMID: 17952575

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