Madan K - Search Results

1

Kabuki syndrome in son and low grade mosaic 45,X/46,XX in mother.

Van Hagen JM, Kwee ML, Madan K, Nieuwint AW, Pals G, ten Kate LP. Van Hagen JM, et al. Among authors: madan k. Genet Couns. 1996;7(3):201-6. Genet Couns. 1996. PMID: 8897041 Review.

2

Recombination in a balanced complex translocation of a mother leading to a balanced reciprocal translocation in the child. Review of 60 cases of balanced complex translocations.

Madan K, Nieuwint AW, van Bever Y. Madan K, et al. Hum Genet. 1997 Jun;99(6):806-15. doi: 10.1007/s004390050453. Hum Genet. 1997. PMID: 9187678 Review.

3

'Identical' twins with discordant karyotypes.

Nieuwint A, Van Zalen-Sprock R, Hummel P, Pals G, Van Vugt J, Van Der Harten H, Heins Y, Madan K. Nieuwint A, et al. Among authors: madan k. Prenat Diagn. 1999 Jan;19(1):72-6. doi: 10.1002/(sici)1097-0223(199901)19:1<72::aid-pd465>3.0.co;2-v. Prenat Diagn. 1999. PMID: 10073913

4

Atypical progeroid syndrome: an unknown helicase gene defect?

Ruijs MW, van Andel RN, Oshima J, Madan K, Nieuwint AW, Aalfs CM. Ruijs MW, et al. Among authors: madan k. Am J Med Genet A. 2003 Jan 30;116A(3):295-9. doi: 10.1002/ajmg.a.10730. Am J Med Genet A. 2003. PMID: 12503110

5

Mosaic tetrasomy 21 in a male child.

Kwee ML, Barth PG, Arwert F, Madan K. Kwee ML, et al. Among authors: madan k. Clin Genet. 1984 Aug;26(2):150-5. doi: 10.1111/j.1399-0004.1984.tb00805.x. Clin Genet. 1984. PMID: 6467667

6

Early prenatal diagnosis of Fanconi anaemia in a twin pregnancy, using DNA analysis.

Kwee ML, Lo Ten Foe JR, Arwert F, Pals G, Madan K, Nieuwint A, In't Veld PA, Van der Horst AR, Van Vugt JM, Ten Kate LP. Kwee ML, et al. Among authors: madan k. Prenat Diagn. 1996 Apr;16(4):345-8. doi: 10.1002/(SICI)1097-0223(199604)16:4<345::AID-PD852>3.0.CO;2-9. Prenat Diagn. 1996. PMID: 8734810

7

[Williams syndrome: new insights into genetic etiology, pathogenesis and clinical aspects].

van Hagen JM, Govaerts LC, de Coo IF, Gille JJ, Nieuwint AW, Madan K. van Hagen JM, et al. Among authors: madan k. Ned Tijdschr Geneeskd. 2001 Mar 3;145(9):396-400. Ned Tijdschr Geneeskd. 2001. PMID: 11253493 Review. Dutch.

8

Rapid detection of microdeletions using fluorescence in situ hybridisation (FISH) on buccal smears.

Nieuwint AW, Van Hagen JM, Heins YM, Madan K, Ten Kate LP. Nieuwint AW, et al. Among authors: madan k. J Med Genet. 2000 Jun;37(6):E4. doi: 10.1136/jmg.37.6.e4. J Med Genet. 2000. PMID: 10851257 Free PMC article. No abstract available.

9

Reproductive risks for paracentric inversion heterozygotes: Inversion or insertion? That is the question.

Madan K, Nieuwint AW. Madan K, et al. Am J Med Genet. 2002 Feb 1;107(4):340-3. doi: 10.1002/ajmg.10173. Am J Med Genet. 2002. PMID: 11840494 Review. No abstract available.

10

Confounding factors in the diagnosis of Fanconi anaemia.

Joenje H, Arwert F, Kwee ML, Madan K, Hoehn H. Joenje H, et al. Among authors: madan k. Am J Med Genet. 1998 Oct 12;79(5):403-5. doi: 10.1002/(sici)1096-8628(19981012)79:5<403::aid-ajmg16>3.0.co;2-v. Am J Med Genet. 1998. PMID: 9779812 No abstract available.

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