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Showing 1 to 12 of 24 entries
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[Epidemiological aspects of birth defects].

Ryoikibetsu shokogun shirizu

Kuroki Y.
PMID: 11529053
Ryoikibetsu Shokogun Shirizu. 2001;(34):845-50.

No abstract available.

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Kuroki Y. [Epidemiological aspects of birth defects]. Ryoikibetsu Shokogun Shirizu. 2001;(34):845-50
Kuroki, Y. (2001). [Epidemiological aspects of birth defects]. Ryoikibetsu shokogun shirizu, (34), 845-50.
Kuroki, Y. "[Epidemiological aspects of birth defects]." Ryoikibetsu shokogun shirizu vol. ,34 (2001): 845-50.
Kuroki Y. [Epidemiological aspects of birth defects]. Ryoikibetsu Shokogun Shirizu. 2001;(34):845-50. Japanese. PMID: 11529053.
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[Polygenic heredity].

Revue medicale de Liege

Lambotte C.
PMID: 5074979
Rev Med Liege. 1972 Jun;27:Suppl 1:19-22.

No abstract available.

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Lambotte C. Hérédité polygénique. [Polygenic heredity]. Rev Med Liege. 1972;27:Suppl 1:19-22
Lambotte, C. (1972). Hérédité polygénique. [Polygenic heredity]. Revue medicale de Liege, 27Suppl 1:19-22.
Lambotte, C. "Hérédité polygénique." [Polygenic heredity]. Revue medicale de Liege vol. 27 (1972): Suppl 1:19-22.
Lambotte C. Hérédité polygénique. [Polygenic heredity]. Rev Med Liege. 1972 Jun;27:Suppl 1:19-22. French. PMID: 5074979.
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Some familial congenital malformations.

Midwives chronicle

Williamson EM.
PMID: 5179695
Midwives Chron. 1966 Oct;79(945):388-9.

No abstract available.

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Williamson EM. Some familial congenital malformations. Midwives Chron. 1966;79(945):388-9
Williamson, E. M. (1966). Some familial congenital malformations. Midwives chronicle, 79(945), 388-9.
Williamson, E M. "Some familial congenital malformations." Midwives chronicle vol. 79,945 (1966): 388-9.
Williamson EM. Some familial congenital malformations. Midwives Chron. 1966 Oct;79(945):388-9. PMID: 5179695.
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[Genetics and congenital abnormalities].

Revue medicale de la Suisse romande

TAILLARD W.
PMID: 13836606
Rev Med Suisse Romande. 1959 Jul;79:449-72.

No abstract available.

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TAILLARD W. [Genetics and congenital abnormalities]. Rev Med Suisse Romande. 1959;79:449-72
TAILLARD, W. (1959). [Genetics and congenital abnormalities]. Revue medicale de la Suisse romande, 79449-72.
TAILLARD, W. "[Genetics and congenital abnormalities]." Revue medicale de la Suisse romande vol. 79 (1959): 449-72.
TAILLARD W. [Genetics and congenital abnormalities]. Rev Med Suisse Romande. 1959 Jul;79:449-72. French. PMID: 13836606.
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Congenital malformation; genetical aspects.

Nordisk medicin

FRACCARO M.
PMID: 13484044
Nord Med. 1957 Sep 26;58(39):1463.

No abstract available.

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FRACCARO M. Congenital malformation; genetical aspects. Congenital malformation; genetical aspects. Nord Med. 1957;58(39):1463
FRACCARO, M. (1957). Congenital malformation; genetical aspects. Congenital malformation; genetical aspects. Nordisk medicin, 58(39), 1463.
FRACCARO, M. "Congenital malformation; genetical aspects." Congenital malformation; genetical aspects. Nordisk medicin vol. 58,39 (1957): 1463.
FRACCARO M. Congenital malformation; genetical aspects. Congenital malformation; genetical aspects. Nord Med. 1957 Sep 26;58(39):1463. PMID: 13484044.
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Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data.

Birth defects research

Jenkins MM, Almli LM, Pangilinan F, Chong JX, Blue EE, Shapira SK, White J, McGoldrick D, Smith JD, Mullikin JC, Bean CJ, Nembhard WN, Lou XY, Shaw GM, Romitti PA, Keppler-Noreuil K, Yazdy MM, Kay DM, Carter TC, Olshan AF, Moore KJ, Nascone-Yoder N, Finnell RH, Lupo PJ, Feldkamp ML, Nickerson DA, Bamshad MJ, Brody LC, Reefhuis J.
PMID: 31328417
Birth Defects Res. 2019 Dec 01;111(20):1618-1632. doi: 10.1002/bdr2.1554. Epub 2019 Jul 21.

BACKGROUND: The National Birth Defects Prevention Study (NBDPS) is a multisite, population-based, case-control study of genetic and nongenetic risk factors for major structural birth defects. Eligible women had a pregnancy affected by a birth defect or a liveborn child...

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Jenkins MM, Almli LM, Pangilinan F, et al. Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data. Birth Defects Res. 2019;111(20):1618-1632doi: 10.1002/bdr2.1554.
Jenkins, M. M., Almli, L. M., Pangilinan, F., Chong, J. X., Blue, E. E., Shapira, S. K., White, J., McGoldrick, D., Smith, J. D., Mullikin, J. C., Bean, C. J., Nembhard, W. N., Lou, X. Y., Shaw, G. M., Romitti, P. A., Keppler-Noreuil, K., Yazdy, M. M., Kay, D. M., Carter, T. C., Olshan, A. F., Moore, K. J., Nascone-Yoder, N., Finnell, R. H., Lupo, P. J., Feldkamp, M. L., Nickerson, D. A., Bamshad, M. J., Brody, L. C., Reefhuis, J. (2019). Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data. Birth defects research, 111(20), 1618-1632. https://doi.org/10.1002/bdr2.1554
Jenkins, Mary M, et al. "Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data." Birth defects research vol. 111,20 (2019): 1618-1632. doi: https://doi.org/10.1002/bdr2.1554
Jenkins MM, Almli LM, Pangilinan F, Chong JX, Blue EE, Shapira SK, White J, McGoldrick D, Smith JD, Mullikin JC, Bean CJ, Nembhard WN, Lou XY, Shaw GM, Romitti PA, Keppler-Noreuil K, Yazdy MM, Kay DM, Carter TC, Olshan AF, Moore KJ, Nascone-Yoder N, Finnell RH, Lupo PJ, Feldkamp ML, Nickerson DA, Bamshad MJ, Brody LC, Reefhuis J. Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data. Birth Defects Res. 2019 Dec 01;111(20):1618-1632. doi: 10.1002/bdr2.1554. Epub 2019 Jul 21. PMID: 31328417; PMCID: PMC6889076.
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Deciphering congenital anomalies for the next generation.

Cold Spring Harbor molecular case studies

Wojcik MH, Agrawal PB.
PMID: 32826208
Cold Spring Harb Mol Case Stud. 2020 Oct 07;6(5). doi: 10.1101/mcs.a005504. Print 2020 Oct.

Congenital anomalies are common, with 2%-3% of infants estimated to have at least one major congenital malformation and countless others with minor malformations of lesser cosmetic or medical importance. As congenital malformations are major drivers of morbidity and mortality,...

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Wojcik MH, Agrawal PB. Deciphering congenital anomalies for the next generation. Cold Spring Harb Mol Case Stud. 2020;6(5)doi: 10.1101/mcs.a005504.
Wojcik, M. H., & Agrawal, P. B. (2020). Deciphering congenital anomalies for the next generation. Cold Spring Harbor molecular case studies, 6(5), . https://doi.org/10.1101/mcs.a005504
Wojcik, Monica H, and Agrawal, Pankaj B. "Deciphering congenital anomalies for the next generation." Cold Spring Harbor molecular case studies vol. 6,5 (2020). doi: https://doi.org/10.1101/mcs.a005504
Wojcik MH, Agrawal PB. Deciphering congenital anomalies for the next generation. Cold Spring Harb Mol Case Stud. 2020 Oct 07;6(5). doi: 10.1101/mcs.a005504. Print 2020 Oct. PMID: 32826208; PMCID: PMC7552931.
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[The significance of genetic factors in congenital malformations].

Ugeskrift for laeger

SCHULTZ-LARSEN J.
PMID: 13748884
Ugeskr Laeger. 1961 Jan 06;123:10-4.

No abstract available.

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SCHULTZ-LARSEN J. [The significance of genetic factors in congenital malformations]. Ugeskr Laeger. 1961;123:10-4
SCHULTZ-LARSEN, J. (1961). [The significance of genetic factors in congenital malformations]. Ugeskrift for laeger, 12310-4.
SCHULTZ-LARSEN, J. "[The significance of genetic factors in congenital malformations]." Ugeskrift for laeger vol. 123 (1961): 10-4.
SCHULTZ-LARSEN J. [The significance of genetic factors in congenital malformations]. Ugeskr Laeger. 1961 Jan 06;123:10-4. Danish. PMID: 13748884.
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The inheritance of common congenital malformations.

Progress in medical genetics

Carter CO.
PMID: 5319121
Prog Med Genet. 1965;4:59-84.

No abstract available.

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Carter CO. The inheritance of common congenital malformations. Prog Med Genet. 1965;4:59-84
Carter, C. O. (1965). The inheritance of common congenital malformations. Progress in medical genetics, 459-84.
Carter, C O. "The inheritance of common congenital malformations." Progress in medical genetics vol. 4 (1965): 59-84.
Carter CO. The inheritance of common congenital malformations. Prog Med Genet. 1965;4:59-84. PMID: 5319121.
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Etiology of malformations.

The New England journal of medicine

Leck I.
PMID: 5825905
N Engl J Med. 1965 Oct 14;273(16):864-6. doi: 10.1056/NEJM196510142731607.

No abstract available.

Cite
Leck I. Etiology of malformations. N Engl J Med. 1965;273(16):864-6doi: 10.1056/NEJM196510142731607.
Leck, I. (1965). Etiology of malformations. The New England journal of medicine, 273(16), 864-6. https://doi.org/10.1056/NEJM196510142731607
Leck, I. "Etiology of malformations." The New England journal of medicine vol. 273,16 (1965): 864-6. doi: https://doi.org/10.1056/NEJM196510142731607
Leck I. Etiology of malformations. N Engl J Med. 1965 Oct 14;273(16):864-6. doi: 10.1056/NEJM196510142731607. PMID: 5825905.
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The fetus and the newborn. Annual review of birth defects, 1980.

Birth defects original article series

[No authors listed]
PMID: 7284578
Birth Defects Orig Artic Ser. 1981;17(1):1-273.

No abstract available.

Cite
The fetus and the newborn. Annual review of birth defects, 1980. Birth Defects Orig Artic Ser. 1981;17(1):1-273
(1981). The fetus and the newborn. Annual review of birth defects, 1980. Birth defects original article series, 17(1), 1-273.
"The fetus and the newborn. Annual review of birth defects, 1980." Birth defects original article series vol. 17,1 (1981): 1-273.
The fetus and the newborn. Annual review of birth defects, 1980. Birth Defects Orig Artic Ser. 1981;17(1):1-273. PMID: 7284578.
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[Congenital anomalies of renal development: genetic and radiological classification].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Salomon R.
PMID: 19541135
Arch Pediatr. 2009 Jun;16(6):698-9. doi: 10.1016/S0929-693X(09)74117-X.

No abstract available.

Cite
Salomon R. Les anomalies du développement rénal: nouvelle classification, << radiologique >>, << génétique >> [Congenital anomalies of renal development: genetic and radiological classification]. Arch Pediatr. 2009;16(6):698-9doi: 10.1016/S0929-693X(09)74117-X.
Salomon, R. (2009). Les anomalies du développement rénal: nouvelle classification, << radiologique >>, << génétique >> [Congenital anomalies of renal development: genetic and radiological classification]. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 16(6), 698-9. https://doi.org/10.1016/S0929-693X(09)74117-X
Salomon, R. "Les anomalies du développement rénal: nouvelle classification, << radiologique >>, << génétique >>" [Congenital anomalies of renal development: genetic and radiological classification]. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 16,6 (2009): 698-9. doi: https://doi.org/10.1016/S0929-693X(09)74117-X
Salomon R. Les anomalies du développement rénal: nouvelle classification, << radiologique >>, << génétique >> [Congenital anomalies of renal development: genetic and radiological classification]. Arch Pediatr. 2009 Jun;16(6):698-9. doi: 10.1016/S0929-693X(09)74117-X. French. PMID: 19541135.
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Showing 1 to 12 of 24 entries