Kwee ML - Search Results

1

Prenatal ultrasound diagnosis of the Holt-Oram syndrome.

Brons JT, van Geijn HP, Wladimiroff JW, van der Harten JJ, Kwee ML, Sobotka-Plojhar M, Arts NF. Brons JT, et al. Among authors: kwee ml. Prenat Diagn. 1988 Mar;8(3):175-81. doi: 10.1002/pd.1970080303. Prenat Diagn. 1988. PMID: 3287365

2

Joubert syndrome: a clinical and pathological description of an affected male and a female fetus from the same sibship.

van Dorp DB, Palan A, Kwee ML, Barth PG, van der Harten JJ. van Dorp DB, et al. Among authors: kwee ml. Am J Med Genet. 1991 Jul 1;40(1):100-4. doi: 10.1002/ajmg.1320400121. Am J Med Genet. 1991. PMID: 1887836 Review.

3

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. 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

4

Mesomelic dysplasia, Kantaputra type: clinical report, prenatal diagnosis, no evidence for SHOX deletion/mutation.

Kwee ML, van de Sluijs JA, van Vugt JM, Wijnaendts LC, Gille JJ. Kwee ML, et al. Am J Med Genet A. 2004 Aug 1;128A(4):404-9. doi: 10.1002/ajmg.a.30120. Am J Med Genet A. 2004. PMID: 15264287

5

Acardius acephalus after induced ovulation: a case report.

Haring DA, Cornel MC, van der Linden JC, van Vugt JM, Kwee ML. Haring DA, et al. Among authors: kwee ml. Teratology. 1993 Apr;47(4):257-62. doi: 10.1002/tera.1420470402. Teratology. 1993. PMID: 8322219

6

Van der Woude syndrome--recognition of lesser expressions: case report.

Menko FH, Koedijk PH, Baart JA, Kwee ML. Menko FH, et al. Among authors: kwee ml. Cleft Palate J. 1988 Jul;25(3):318-21. Cleft Palate J. 1988. PMID: 3168277

7

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: kwee ml. Genet Couns. 1996;7(3):201-6. Genet Couns. 1996. PMID: 8897041 Review.

8

Kabuki syndrome - report of six cases and review of the literature with emphasis on ocular features.

Kluijt I, van Dorp DB, Kwee ML, Toutain A, Keppler-Noreuil K, Warburg M, Bitoun P. Kluijt I, et al. Among authors: kwee ml. Ophthalmic Genet. 2000 Mar;21(1):51-61. Ophthalmic Genet. 2000. PMID: 10779849 Review.

9

Tuberous sclerosis. Diagnostic problems in a family.

van Dorp DB, Kwee ML. van Dorp DB, et al. Among authors: kwee ml. Ophthalmic Paediatr Genet. 1990 Jun;11(2):95-101. doi: 10.3109/13816819009012953. Ophthalmic Paediatr Genet. 1990. PMID: 2377357

10

Mosaic tetrasomy 21 in a male child.

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

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