Crandall BF - Search Results

1

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: crandall bf. Am J Hum Genet. 1997 Apr;60(4):935-47. Am J Hum Genet. 1997. PMID: 9106541 Free PMC article.

2

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: crandall bf. J Genet Couns. 1994 Dec;3(4):279-89. doi: 10.1007/BF01412373. J Genet Couns. 1994. PMID: 24234134

3

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: crandall bf. Womens Health. 1997 Spring;3(1):31-51. Womens Health. 1997. PMID: 9106369

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: crandall bf. Am J Med Genet. 1998 Nov 16;80(3):247-51. Am J Med Genet. 1998. PMID: 9843047

5

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

Jam K, Fox M, Crandall BF. Jam K, et al. Among authors: crandall bf. 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.

6

Trisomy 18 mosaicism: clues to the diagnosis.

Bass HN, Fox M, Wulfsberg E, Sparkes RS, Crandall BF. Bass HN, et al. Among authors: crandall bf. Clin Genet. 1982 Dec;22(6):327-30. doi: 10.1111/j.1399-0004.1982.tb01848.x. Clin Genet. 1982. PMID: 7160104

7

Prenatal diagnosis of glucose-6-phosphate-dehydrogenase deficiency.

Beutler E, Kuhl W, Fox M, Tabsh K, Crandall BF. Beutler E, et al. Among authors: crandall bf. Acta Haematol. 1992;87(1-2):103-4. doi: 10.1159/000204729. Acta Haematol. 1992. PMID: 1316704

8

The tirsomy 8 syndrome: two additional mosaic cases.

Crandall BF, Bass HN, Marcy SM, Glovsky M, Fish CH. Crandall BF, et al. J Med Genet. 1974 Dec;11(4):393-8. doi: 10.1136/jmg.11.4.393. J Med Genet. 1974. PMID: 4443989 Free PMC article.

9

Two different chromosome abnormalities resulting from a translocation carrier father.

Bass HN, Crandall BF, Marcy SM. Bass HN, et al. Among authors: crandall bf. J Pediatr. 1973 Dec;83(6):1034-8. doi: 10.1016/s0022-3476(73)80545-1. J Pediatr. 1973. PMID: 4757516 No abstract available.

10

Partial trisomy of chromosome number 15 identified by trypsin-Giemsa banding.

Crandall BF, Muller HM, Bass HN. Crandall BF, et al. Am J Ment Defic. 1973 Mar;77(5):571-8. Am J Ment Defic. 1973. PMID: 4703990 No abstract available.

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