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Items: 1 to 20 of 96

1.
2.

Familial occurrence of lumbar spondylolysis and spondylolisthesis.

Haukipuro K, Keränen N, Koivisto E, Lindholm R, Norio R, Punto L.

Clin Genet. 1978 Jun;13(6):471-6.

PMID:
668183
3.
4.

The genetics of spina bifida occulta.

Laurence KM.

Dev Med Child Neurol. 1967 Oct;9(5):645-6. No abstract available.

PMID:
4863976
5.

Spinal dysraphia as an autosomal dominant defect in four families.

Fineman RM, Jorde LB, Martin RA, Hasstedt SJ, Wing SD, Walker ML.

Am J Med Genet. 1982 Aug;12(4):457-64.

PMID:
6751087
6.

Microsatellites proximal to leptin and leptin receptor as risk factors for spina bifida.

Shaw GM, Barber R, Todoroff K, Lammer EJ, Finnell RH.

Teratology. 2000 Mar;61(3):231-5.

PMID:
10661913
7.

[Spina bifida occulta and other neural tube defects. Genetic study and management].

Robert E.

Neurochirurgie. 1988;34 Suppl 1:87-90. French. No abstract available.

PMID:
3054614
8.

Outcome of meningomyelocele/lipomeningomyelocele in children of northern India.

Kumar R, Singhal N.

Pediatr Neurosurg. 2007;43(1):7-14.

PMID:
17190981
9.

A genetic study of spina bifida cystica in Utah.

Woolf CM.

Soc Biol. 1975 Fall;22(3):216-20. No abstract available.

PMID:
766191
10.

Familial incidence of osseous lesions in neurofibromatosis.

Agarwal RP, Goel MK.

J Indian Med Assoc. 1980 Mar 1;74(5):93-4. No abstract available.

PMID:
6774026
11.

The impact of BRCA1 on spina bifida meningomyelocele lesions.

King TM, Au KS, Kirkpatrick TJ, Davidson C, Fletcher JM, Townsend I, Tyerman GH, Shimmin LC, Northrup H.

Ann Hum Genet. 2007 Nov;71(Pt 6):719-28. Epub 2007 Jul 19.

12.

Congenital absence of gluteal muscles. Report of two sibs.

Carnevale A, del Castillo V, Sotillo AG, Larrondo J.

Clin Genet. 1976 Sep;10(3):135-8.

PMID:
786514
13.

Guadalajara camptodactyly type III: a new probably autosomal dominant syndrome.

Figuera LE, Ramírez-Dueñas ML, Dávalos IP, Cantú JM.

Clin Dysmorphol. 2002 Oct;11(4):243-7.

PMID:
12401988
14.

Apparently monogenic inheritance of anencephaly and spina bifida in a kindred.

Fuhrmann W, Seeger W, Böhm R.

Humangenetik. 1971;13(3):241-3. No abstract available.

PMID:
4939953
15.

Family study of spondylolysis and spondylolisthesis.

Albanese M, Pizzutillo PD.

J Pediatr Orthop. 1982;2(5):496-9.

PMID:
6761366
16.

Brief communication: possible X-linked anencephaly and spina bifida--report of a kindred.

Toriello HV, Warren ST, Lindstrom JA.

Am J Med Genet. 1980;6(2):119-21.

PMID:
7004185
17.

Familial spina bifida associated with antiemetic ingestion in the first semester.

Walker FA.

Birth Defects Orig Artic Ser. 1974;10(7):17-21. No abstract available.

PMID:
4608486
18.

Vertebral and other abnormalities in parents and sibs of cases of spina bifida cystica and of anencephaly.

Laurence KM, Bligh AS, Evans KT.

Dev Med Child Neurol. 1968:Suppl 16:107+. No abstract available.

PMID:
4896353
19.

The frequency of spina bifida occulta and rib anomalies in the parents of children with spina bifida aperta and meningocoele.

MILLER JR, FRASER FC, MACEWAN DW.

Am J Hum Genet. 1962 Sep;14:245-8. No abstract available.

20.

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

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