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Results: 1 to 20 of 104

1.

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

Jam K, Fox M, Crandall BF.

Teratology. 1999 Jul;60(1):37-8. No abstract available.

PMID:
10413338
[PubMed - indexed for MEDLINE]
2.

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.

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

PMID:
9843047
[PubMed - indexed for MEDLINE]
3.

Congenital olivopontocerebellar atrophy: report of two siblings with paleo- and neocerebellar atrophy.

Park SH, Becker-Catania S, Gatti RA, Crandall BF, Emelin JK, Vinters HV.

Acta Neuropathol. 1998 Oct;96(4):315-21.

PMID:
9796994
[PubMed - indexed for MEDLINE]
4.

American College of Medical Genetics statement on folic acid: fortification and supplementation.

Crandall BF, Corson VL, Evans MI, Goldberg JD, Knight G, Salafsky IS.

Am J Med Genet. 1998 Jul 24;78(4):381. No abstract available.

PMID:
9714444
[PubMed - indexed for MEDLINE]
5.

Significance of fetal intracardiac echogenic foci in relation to trisomy 21: a prospective sonographic study of high-risk pregnant women.

Manning JE, Ragavendra N, Sayre J, Laifer-Narin SL, Melany ML, Grant EG, Crandall BF.

AJR Am J Roentgenol. 1998 Apr;170(4):1083-4.

PMID:
9530064
[PubMed - indexed for MEDLINE]
6.

Risks for fetal abnormalities after very and moderately elevated AF-AFPs.

Crandall BF, Chua C.

Prenat Diagn. 1997 Sep;17(9):837-41.

PMID:
9316128
[PubMed - indexed for MEDLINE]
7.

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.

Am J Hum Genet. 1997 Apr;60(4):935-47.

PMID:
9106541
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

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.

Womens Health. 1997 Spring;3(1):31-51.

PMID:
9106369
[PubMed - indexed for MEDLINE]
9.

Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.

Hsu LY, Yu MT, Richkind KE, Van Dyke DL, Crandall BF, Saxe DF, Khodr GS, Mennuti M, Stetten G, Miller WA, Priest JH.

Prenat Diagn. 1996 Jan;16(1):1-28.

PMID:
8821848
[PubMed - indexed for MEDLINE]
10.

Preliminary phenotypic map of chromosome 4p16 based on 4p deletions.

Estabrooks LL, Rao KW, Driscoll DA, Crandall BF, Dean JC, Ikonen E, Korf B, Aylsworth AS.

Am J Med Genet. 1995 Jul 17;57(4):581-6.

PMID:
7573133
[PubMed - indexed for MEDLINE]
11.

Coloboma associated with Rubinstein-Taybi syndrome.

Ge N, Crandall BF, Shuler JD, Bateman JB.

J Pediatr Ophthalmol Strabismus. 1995 Jul-Aug;32(4):266-8. No abstract available.

PMID:
7494168
[PubMed - indexed for MEDLINE]
12.

Detecting neural tube defects by amniocentesis between 11 and 15 weeks' gestation.

Crandall BF, Chua C.

Prenat Diagn. 1995 Apr;15(4):339-43.

PMID:
7542382
[PubMed - indexed for MEDLINE]
13.

Folic acid and pregnancy.

Crandall BF, Corson VL, Goldberg JD, Knight G, Salafsky IS.

Am J Med Genet. 1995 Jan 2;55(1):134-5. No abstract available.

PMID:
7702087
[PubMed - indexed for MEDLINE]
14.

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.

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

PMID:
24234134
[PubMed]
15.

Risk assessment of amniocentesis between 11 and 15 weeks: comparison to later amniocentesis controls.

Crandall BF, Kulch P, Tabsh K.

Prenat Diagn. 1994 Oct;14(10):913-9.

PMID:
7534922
[PubMed - indexed for MEDLINE]
16.

The association between 'faint-positive' amniotic fluid acetylcholinesterase and fetal malformations.

Sadovsky Y, Robbin ML, Crandall BF, Filly RA, Golbus MS.

Prenat Diagn. 1993 Nov;13(11):1071-4.

PMID:
8140072
[PubMed - indexed for MEDLINE]
17.

Maternal serum screening for alpha-fetoprotein, unconjugated estriol, and human chorionic gonadotropin between 11 and 15 weeks of pregnancy to detect fetal chromosome abnormalities.

Crandall BF, Hanson FW, Keener S, Matsumoto M, Miller W.

Am J Obstet Gynecol. 1993 Jun;168(6 Pt 1):1864-7; discussion 1867-9.

PMID:
7686337
[PubMed - indexed for MEDLINE]
18.

Racial differences in maternal serum human chorionic gonadotropin and unconjugated oestriol levels.

Kulch P, Keener S, Matsumoto M, Crandall BF.

Prenat Diagn. 1993 Mar;13(3):191-5.

PMID:
7685088
[PubMed - indexed for MEDLINE]
19.

Ocular manifestations of the lacrimo-auriculo-dento-digital syndrome.

Heinz GW, Bateman JB, Barrett DJ, Thangavel M, Crandall BF.

Am J Ophthalmol. 1993 Feb 15;115(2):243-8.

PMID:
8430736
[PubMed - indexed for MEDLINE]
20.

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