Verjaal M[Author] - Search Results

Year	Number of Results
1977	1
1978	4
1979	2
1980	2
1981	2
1982	1
1984	1
1985	3
1987	3
1988	1
1989	1
1990	2
1992	1
1994	2
1996	1
1999	1
2000	1
2002	1
2024	0

1

Zondervan HA, Verjaal M, Kuegt AC. Zondervan HA, et al. Among authors: verjaal m. Ultrasound Obstet Gynecol. 1999 Feb;13(2):150. doi: 10.1046/j.1469-0705.1999.13020150.x. Ultrasound Obstet Gynecol. 1999. PMID: 10079498 Free article. No abstract available.

2

Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia.

Mannens M, Hoovers JM, Redeker E, Verjaal M, Feinberg AP, Little P, Boavida M, Coad N, Steenman M, Bliek J, et al. Mannens M, et al. Among authors: verjaal m. Eur J Hum Genet. 1994;2(1):3-23. doi: 10.1159/000472337. Eur J Hum Genet. 1994. PMID: 7913866

3

Familial occurrence of azoospermia and extreme oligozoospermia.

Budde WJ, Verjaal M, Hamerlynck JV, Bobrow M. Budde WJ, et al. Among authors: verjaal m. Clin Genet. 1984 Dec;26(6):555-62. doi: 10.1111/j.1399-0004.1984.tb01103.x. Clin Genet. 1984. PMID: 6499267

4

Oligohydramnios hampering prenatal diagnosis of Meckel syndrome.

Verjaal M, Meyer AH, Becker-Bloemkolk MJ, Leschot NJ, der Weduwen JJ, Gras JG. Verjaal M, et al. Am J Med Genet. 1980;7(1):85-6. doi: 10.1002/ajmg.1320070112. Am J Med Genet. 1980. PMID: 7211955 No abstract available.

5

Women's experiences with second trimester prenatal diagnosis.

Verjaal M, Leschot NJ, Treffers PE. Verjaal M, et al. Prenat Diagn. 1982 Jul;2(3):195-209. doi: 10.1002/pd.1970020309. Prenat Diagn. 1982. PMID: 7145848

6

Trisomy 13 or 18 (mosaicism) in first trimester cytotrophoblast cells: false-positive results in 11 out of 51 cases.

Schuring-Blom GH, Boer K, Knegt AC, Verjaal M, Leschot NJ. Schuring-Blom GH, et al. Among authors: verjaal m. Eur J Obstet Gynecol Reprod Biol. 2002 Mar 10;101(2):161-8. doi: 10.1016/s0301-2115(00)00542-x. Eur J Obstet Gynecol Reprod Biol. 2002. PMID: 11858892

7

Prenatal HLA-matching to determine suitability for allogeneic bone marrow transplantation.

van den Berg H, Verjaal M, Boer K, Lardy NM. van den Berg H, et al. Among authors: verjaal m. Bone Marrow Transplant. 2000 Mar;25(6):579-81. doi: 10.1038/sj.bmt.1702219. Bone Marrow Transplant. 2000. PMID: 10734290

8

A patient with a partial deletion of the short arm of chromosome 3.

Verjaal M, De Nef MB. Verjaal M, et al. Am J Dis Child. 1978 Jan;132(1):43-5. doi: 10.1001/archpedi.1978.02120260045012. Am J Dis Child. 1978. PMID: 623063

9

Prenatal diagnosis of congenital malformations in 500 pregnancies.

Leschot NJ, Treffers PE, Verjaal M, der Weduwen JJ, Bennebroek Gravenhorst J, Coelingh Bennink HJ. Leschot NJ, et al. Among authors: verjaal m. Eur J Obstet Gynecol Reprod Biol. 1979 Feb;9(1):13-22. doi: 10.1016/0028-2243(79)90040-6. Eur J Obstet Gynecol Reprod Biol. 1979. PMID: 570519 No abstract available.

10

Rapid prenatal diagnosis of HG-PRT deficiency using ultra-microchemical methods.

Hösli P, de Bruyn CH, Oerlemans FJ, Verjaal M, Nobrega RE. Hösli P, et al. Among authors: verjaal m. Hum Genet. 1977 Jun 30;37(2):195-200. doi: 10.1007/BF00393582. Hum Genet. 1977. PMID: 885539

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