Buntinx I - Search Results

1

Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: characterization by fluorescence in situ hybridization and DNA analysis.

Mangelschots K, Van Roy B, Speleman F, Van Roy N, Gheuens J, Beuten J, Buntinx I, Van Thienen MN, Willekens H, Dumon J, et al. Mangelschots K, et al. Among authors: buntinx i. Hum Genet. 1992 Jun;89(4):407-13. doi: 10.1007/BF00194312. Hum Genet. 1992. PMID: 1352272

2

Molecular study of chromosome 15 in 22 patients with Angelman syndrome.

Beuten J, Mangelschots K, Buntinx I, Coucke P, Brouwer OF, Hennekam RC, Van Broeckhoven C, Willems PJ. Beuten J, et al. Among authors: buntinx i. Hum Genet. 1993 Jan;90(5):489-95. doi: 10.1007/BF00217446. Hum Genet. 1993. PMID: 8094063

3

Clinical profile of Angelman syndrome at different ages.

Buntinx IM, Hennekam RC, Brouwer OF, Stroink H, Beuten J, Mangelschots K, Fryns JP. Buntinx IM, et al. Am J Med Genet. 1995 Mar 27;56(2):176-83. doi: 10.1002/ajmg.1320560213. Am J Med Genet. 1995. PMID: 7625442

4

Robertsonian translocation and an extra microchromosome: independent origin identified by in situ hybridisation.

Mangelschots K, Van Roy B, Buntinx I. Mangelschots K, et al. Among authors: buntinx i. Clin Genet. 1991 Jul;40(1):62. doi: 10.1111/j.1399-0004.1991.tb03069.x. Clin Genet. 1991. PMID: 1884520 No abstract available.

5

Neonatal Marfan syndrome with congenital arachnodactyly, flexion contractures, and severe cardiac valve insufficiency.

Buntinx IM, Willems PJ, Spitaels SE, Van Reempst PJ, De Paepe AM, Dumon JE. Buntinx IM, et al. J Med Genet. 1991 Apr;28(4):267-73. doi: 10.1136/jmg.28.4.267. J Med Genet. 1991. PMID: 1856834 Free PMC article.

6

Acardiac amorphous twin with prune belly sequence in the co-twin.

Buntinx IM, Bourgeois N, Buytaert PM, Dumon JE. Buntinx IM, et al. Am J Med Genet. 1991 Jun 15;39(4):453-7. doi: 10.1002/ajmg.1320390416. Am J Med Genet. 1991. PMID: 1877624

7

A new association of mental retardation, short stature, unusual face, radio-ulnar synostosis and retinal pigment abnormalities.

Buntinx IM, Lormans JA, Martin JJ, Dumon JE. Buntinx IM, et al. Genet Couns. 1991;2(4):237-40. Genet Couns. 1991. PMID: 1799423 No abstract available.

8

Two siblings with midline field defects and Hirschsprung disease: variable expression of Toriello-Carey or new syndrome?

Jespers A, Buntinx I, Melis K, Vaerenberg M, Janssens G. Jespers A, et al. Among authors: buntinx i. Am J Med Genet. 1993 Aug 15;47(2):299-302. doi: 10.1002/ajmg.1320470232. Am J Med Genet. 1993. PMID: 8213924 Review.

9

A single maxillary incisor as a manifestation of an ectodermal dysplasia.

Buntinx I, Baraitser M. Buntinx I, et al. J Med Genet. 1989 Oct;26(10):648-51. doi: 10.1136/jmg.26.10.648. J Med Genet. 1989. PMID: 2585463 Free PMC article.

10

Blepharophimosis, iris coloboma, microgenia, hearing loss, postaxial polydactyly, aplasia of corpus callosum, hydroureter, and developmental delay.

Buntinx I, Majewski F. Buntinx I, et al. Am J Med Genet. 1990 Jul;36(3):273-4. doi: 10.1002/ajmg.1320360304. Am J Med Genet. 1990. PMID: 1694631 No abstract available.

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