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Items: 1 to 50 of 169

1.

Apparent prevention of neural tube defects by periconceptional vitamin supplementation. 1981.

Smithells RW, Sheppard S, Schorah CJ, Seller MJ, Nevin NC, Harris R, Read AP, Fielding DW.

Int J Epidemiol. 2011 Oct;40(5):1146-54. doi: 10.1093/ije/dyr143.

PMID:
22039189
2.

Multicolor banding detects a complex three chromosome, seven breakpoint unbalanced rearrangement in an ICSI-derived fetus with multiple abnormalities.

Seller MJ, Bint S, Kavalier F, Brown RN, Ogilvie CM.

Am J Med Genet A. 2006 May 15;140(10):1102-7.

PMID:
16596677
3.

Six1 and Six4 homeoproteins are required for Pax3 and Mrf expression during myogenesis in the mouse embryo.

Grifone R, Demignon J, Houbron C, Souil E, Niro C, Seller MJ, Hamard G, Maire P.

Development. 2005 May;132(9):2235-49. Epub 2005 Mar 23.

4.

Trisomy 16 in a mid-trimester IVF foetus with multiple abnormalities.

Seller MJ, Fear C, Kumar A, Mohammed S.

Clin Dysmorphol. 2004 Jul;13(3):187-9.

PMID:
15194958
5.

A trisomy 2 fetus with severe neural tube defects and other abnormalities.

Seller MJ, Mazzaschi R, Ogilvie CM, Mohammed S.

Clin Dysmorphol. 2004 Jan;13(1):25-7.

PMID:
15127760
6.

Microdeletion 22q11.2, Kousseff syndrome and spina bifida.

Seller MJ, Mohammed S, Russell J, Ogilvie C.

Clin Dysmorphol. 2002 Apr;11(2):113-5.

PMID:
12002140
8.

Physical and transcript map of the dominant optic atrophy (OPA1) gene critical region at 3q28-q29.

Behnam JT, Hamer C, Spalton D, Johnston R, Seller MJ.

Genomics. 2001 Mar 1;72(2):213-6.

PMID:
11401435
9.

Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral anophthalmia and pituitary anomalies.

Gallardo ME, Lopez-Rios J, Fernaud-Espinosa I, Granadino B, Sanz R, Ramos C, Ayuso C, Seller MJ, Brunner HG, Bovolenta P, Rodríguez de Córdoba S.

Genomics. 1999 Oct 1;61(1):82-91.

PMID:
10512683
10.

Dominant optic atrophy. Refining the clinical diagnostic criteria in light of genetic linkage studies.

Johnston RL, Seller MJ, Behnam JT, Burdon MA, Spalton DJ.

Ophthalmology. 1999 Jan;106(1):123-8.

PMID:
9917792
11.

Altered smooth muscle development and innervation in the lower genitourinary and gastrointestinal tract of the male human fetus with myelomeningocele.

Shapiro E, Seller MJ, Lepor H, Kalousek DK, Hutchins GM, Perlman EJ, Meuli M.

J Urol. 1998 Sep;160(3 Pt 2):1047-53; discussion 1079.

PMID:
9719274
12.

Cervical ribs in mid-trimester fetuses.

Seller MJ.

Am J Med Genet. 1998 Jul 24;78(4):391-2. No abstract available.

PMID:
9714448
13.

Trisomy 9 in an embryo with spina bifida.

Seller MJ, Bergbaum A, Daker MG.

Clin Dysmorphol. 1998 Jul;7(3):217-9.

PMID:
9689998
14.

Cerebellar hypoplasia, facial dysmorphism and internal abnormalities: a new recessive syndrome?

Seller MJ, Pal K, Moscoso G, Nicolaides K, Hyett JA.

Clin Dysmorphol. 1998 Jan;7(1):41-4.

PMID:
9546829
15.

Linkage studies in dominant optic atrophy, Kjer type: possible evidence for heterogeneity.

Seller MJ, Behnam JT, Lewis CM, Johnston RL, Burdon MA, Spalton DJ.

J Med Genet. 1997 Dec;34(12):967-72.

16.

Rapid identification of multiple supernumerary ring chromosomes with a new FISH technique.

Mackie-Ogilvie C, Waddle K, Mandeville J, Seller MJ, Docherty Z.

J Med Genet. 1997 Nov;34(11):912-6.

17.

Terathanasia, folic acid, and birth defects.

Schorah CJ, Smithells RW, Seller MJ.

Lancet. 1997 Nov 1;350(9087):1323; author reply 1323-4. No abstract available.

PMID:
9357425
18.

The spinal cord lesion in human fetuses with myelomeningocele: implications for fetal surgery.

Meuli M, Meuli-Simmen C, Hutchins GM, Seller MJ, Harrison MR, Adzick NS.

J Pediatr Surg. 1997 Mar;32(3):448-52.

PMID:
9094015
19.

Phenotypic diversity in the Smith-Lemli-Opitz syndrome.

Seller MJ, Flinter FA, Docherty Z, Fagg N, Newbould M.

Clin Dysmorphol. 1997 Jan;6(1):69-73.

PMID:
9018421
20.

Dominant optic atrophy, Kjer type. Linkage analysis and clinical features in a large British pedigree.

Johnston RL, Burdon MA, Spalton DJ, Bryant SP, Behnam JT, Seller MJ.

Arch Ophthalmol. 1997 Jan;115(1):100-3. Erratum in: Arch Ophthalmol 1997 May;115(5):681.

PMID:
9006433
21.

Evolution of sonographic findings in a fetus with agenesis of the urethra, vagina, and rectum.

Carroll SG, Hyett J, Eustace D, Seller MJ, Nicolaides KH.

Prenat Diagn. 1996 Oct;16(10):931-3.

PMID:
8938063
22.

A new lethal chondrodysplasia with platyspondyly, long bone angulation and mixed bone density.

Seller MJ, Berry AC, Maxwell D, McLennan A, Hall CM.

Clin Dysmorphol. 1996 Jul;5(3):213-5.

PMID:
8818449
23.

Esophageal and duodenal atresia in a fetus with Down's syndrome: prenatal sonographic features.

Chitty LS, Goodman J, Seller MJ, Maxwell D.

Ultrasound Obstet Gynecol. 1996 Jun;7(6):450-2.

24.

Two sibs with anophthalmia and pulmonary hypoplasia (the Matthew-Wood syndrome).

Seller MJ, Davis TB, Fear CN, Flinter FA, Ellis I, Gibson AG.

Am J Med Genet. 1996 Mar 29;62(3):227-29.

PMID:
8882778
25.

Ultrastructural changes in 9-day old mouse embryos following maternal tobacco smoke inhalation.

Bnait KS, Seller MJ.

Exp Toxicol Pathol. 1995 Dec;47(6):453-61.

PMID:
8871084
26.

Dietary methionine does not reduce penetrance in curly tail mice but causes a phenotype-specific decrease in embryonic growth.

van Straaten HW, Blom H, Peeters MC, Rousseau AM, Cole KJ, Seller MJ.

J Nutr. 1995 Nov;125(11):2733-40.

PMID:
7472652
27.

Double trisomies.

Seller MJ, Mullarkey M, Daker MG.

Clin Dysmorphol. 1995 Oct;4(4):364-5. No abstract available.

PMID:
8574429
28.

Sex, neural tube defects, and multisite closure of the human neural tube.

Seller MJ.

Am J Med Genet. 1995 Sep 25;58(4):332-6.

PMID:
8533841
29.

Multi-site neural tube closure in humans and maternal folate supplementation.

Seller MJ.

Am J Med Genet. 1995 Sep 11;58(3):222-4.

PMID:
8533821
30.

Effects of tobacco smoke inhalation on the developing mouse embryo and fetus.

Seller MJ, Bnait KS.

Reprod Toxicol. 1995 Sep-Oct;9(5):449-59.

PMID:
8563188
31.

A fetus with an X;1 balanced reciprocal translocation and eye disease.

Seller MJ, Pal K, Horsley S, Davies AF, Berry AC, Meredith R, McCartney AC.

J Med Genet. 1995 Jul;32(7):557-60.

32.
33.

Unusual case of Smith-Lemli-Opitz syndrome "type II".

Seller MJ, Russell J, Tint GS.

Am J Med Genet. 1995 Apr 10;56(3):265-8.

PMID:
7778586
34.

Recent developments in the understanding of the aetiology of neural tube defects.

Seller MJ.

Clin Dysmorphol. 1995 Apr;4(2):93-104. Review. No abstract available.

PMID:
7606328
35.
36.

Risks in spina bifida.

Seller MJ.

Dev Med Child Neurol. 1994 Nov;36(11):1021-5. Review. No abstract available.

PMID:
7958508
37.

Fetus with features of Crane-Heise syndrome and aminopterin syndrome sine aminopterin (ASSAS).

Barnicoat AJ, Seller MJ, Bennett CP.

Clin Dysmorphol. 1994 Oct;3(4):353-7.

PMID:
7894742
38.

Investigation of folate intake and metabolism in women who have had two pregnancies complicated by neural tube defects.

Wild J, Seller MJ, Schorah CJ, Smithells RW.

Br J Obstet Gynaecol. 1994 Mar;101(3):197-202.

PMID:
8193092
39.

A fetus with an abnormal chromosome 7 and possible hydrolethalus syndrome.

Seller MJ, Pal K, Docherty Z, Nash TG.

Clin Dysmorphol. 1994 Jan;3(1):35-9.

PMID:
8205324
40.

Vitamins, folic acid and the cause and prevention of neural tube defects.

Seller MJ.

Ciba Found Symp. 1994;181:161-73; discussion 173-9. Review.

PMID:
8005023
41.

Pseudotrisomy 13 and autosomal recessive holoprosencephaly.

Seller MJ, Chitty LS, Dunbar H.

J Med Genet. 1993 Nov;30(11):970-1.

42.
44.

Uptake and utilization of DL-5-[methyl-14C] tetrahydropteroylmonoglutamate by cultured cytotrophoblasts associated with neural tube defects.

Habibzadeh N, Schorah CJ, Seller MJ, Smithells RW, Levene MI.

Proc Soc Exp Biol Med. 1993 May;203(1):45-54.

PMID:
8475138
45.

The human embryo: a scientist's point of view.

Seller MJ.

Bioethics. 1993 Apr;7(2-3):135-40.

PMID:
11651526
46.

Possible abnormalities of folate and vitamin B12 metabolism associated with neural tube defects.

Schorah CJ, Habibzadeh N, Wild J, Smithells RW, Seller MJ.

Ann N Y Acad Sci. 1993 Mar 15;678:81-91. No abstract available.

PMID:
8494295
47.

Acrocallosal syndrome and 12p.

Docherty Z, Seller MJ.

Ann Genet. 1993;36(2):136. No abstract available.

PMID:
8215222
48.

Chondrodysplasia punctata: another possible X-linked recessive case.

Bennett CP, Berry AC, Maxwell DJ, Seller MJ.

Am J Med Genet. 1992 Dec 1;44(6):795-9.

PMID:
1481849
49.

Trisomy 15 mosaicism in an IVF fetus.

Bennett CP, Davis T, Seller MJ.

J Med Genet. 1992 Oct;29(10):745-6.

50.

Pancreatic and sacral agenesis in association with maternal diabetes mellitus: case report.

Johnson P, Seller MJ, Morrish N, Neales K, Maxwell D.

Prenat Diagn. 1991 May;11(5):329-31. No abstract available.

PMID:
1896419

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