Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome.
about
Trisomy 13 and extended survival.Clinical experience with trisomies 18 and 13.Genetic heterogeneity of cebocephaly.Diaphragmatic hernia in the south-west of EnglandFamilial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomyPartial trisomy 18 in a family with a translocation (18;21)(q21;q22).Intraocular pathology of trisomy 18 (Edwards's syndrome): report of a case and review of the literature.The eye in the CHARGE association.Syndrome of polydactyly, cleft lip/palate or lingual lump, and psychomotor retardation in endogamic gypsies.Clinical manifestations of familial 13;18 translocation.The aetiology of the cat eye syndrome reconsidered.Four cases of trisomy 18 syndrome with limb reduction malformationsHoloprosencephaly in the west of Scotland 1975-1994.Defective migration of neuroendocrine GnRH cells in human arrhinencephalic conditions.Preaxial polydactyly of the foot: variable expression of trisomy 13 in a case from central Africa.Craniofacial abnormalities among patients with Edwards Syndrome.Gestational, perinatal and family findings of patients with Patau syndrome.Leatherwork: a possible hazard to reproductionRetinoblastoma and deletion D (14) syndrome.Wolf-Hirschhorn syndrome associated with an unusual abnormality of chromosome no. 4.Developmental abnormalities in a patient with karyotype 46,XX,bq+.Trisomy E and T-E fistula.Trisomy E (18) syndrome: clinical spectrum in 12 new cases, including chromosome autoradiography in 4.Trisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliography.A case of partial 14 trisomy 47,XY,(14q-)+ and translocation t(9p+;14q-) in mother and brotherTrisomy 18 in one of fraternal twinsPolycystic disease of kidney and liver presenting in childhoodMongolism and sex: a common problem of cell proliferation?Longevity and Patau syndrome: what determines survival?Dental defects associated with neonatal symptomatic hypocalcaemiaCongenital malformations of human dermatoglyphsGenetics of atrial septal defect.Chromosome studies in investigation of stillbirths and neonatal deaths.Double aneuploidy: the frequency of XXY in males with Down's syndrome.Studies on chromosomal nondisjunction in man. 3.The 13q-deletion syndrome.Trisomy 13 with a 13-X translocation.Banding analysis of abnormal karyotypes in spontaneous abortion.Age trends in human chiasma frequencies and recombination fractions. I. Chiasma frequencies.Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21)
P2860
Q33584853-BFB5F50C-51D5-45EF-AD7E-B66FC847C17EQ33585106-8FE28D3E-D0B2-430E-B005-B87FB401F10AQ33585937-D4E9C2F0-3F4F-403A-A4E6-1937FD2EC10AQ33587017-4C069947-3229-414E-B586-ADBA9F4D5304Q33587439-19349FCD-FD41-44B9-9D8A-A3C791F19976Q33588045-D367B30B-518C-4CA1-B6F1-C966F99551B6Q33642454-6ADCF020-4585-425A-A8F9-C815ECE35C22Q33648152-E2DA7E1F-EF2E-4017-AD67-1F943D77AFE5Q33667814-27AF013A-7511-4F37-BDD3-D165E7EC1267Q33668281-840D87A6-FE12-4C7E-BA0A-BFE5EE6FD911Q33668547-CA828FAC-4EBF-4C73-83E8-4FC07EE64D4CQ33671480-682D8B7F-E8CF-412C-919B-B2846706ACBCQ33677544-77E4DE2E-4546-402E-9BA0-B9DC9A4BE0F5Q34162228-50FAD6F8-ACCD-4B7D-BBF1-1C1078969E48Q34183027-9459C7B7-532B-4B54-B03E-F5888BD1AA20Q34279300-8E3674DD-097D-4A6B-BE42-56EF857F0BE5Q34279628-E87B0984-0CD5-4400-BBAB-47718732E5C8Q34485131-3683ABC9-1543-4CD7-B5F0-83D375EC3E04Q34633401-87A1FA77-7E9A-401E-B667-A8AF6550D17CQ34633620-3CD5B856-67DA-483B-94C0-69EAEADB95A8Q34633643-B10D7C02-A5E9-4E31-AFAB-A2BD1CBD9F76Q34633971-9FF16ED8-D6F9-4003-8581-960B6614C9D7Q34634055-DC842F93-A7ED-46EE-AA34-34F3CC803C8AQ34634568-9C7CBC5C-BA5B-4384-B951-FD3B6DE15A7CQ34634879-F8313350-1418-4B62-AFC5-92C5E010EAD6Q34635022-ABD63BC4-9745-4E85-903F-AEB5A0D2C4F2Q34635045-E42ED567-993D-4461-A408-CD80AAF64818Q34635220-A9592761-F0F4-42AE-813D-5B72D67E60E1Q34646143-4B68CE8D-EECE-4719-8A0B-191B172909B1Q35149693-6F50765D-A908-434F-9936-5742F85FF49FQ35149698-CAE2A52C-1654-4BC3-AEC0-1AD44F8A312DQ35150152-DC5290F8-4267-4084-9957-2545B4EC4D74Q35151820-A51C9452-B7C8-4311-A278-A41CDD647A56Q35231943-8F0D917E-92BF-45DE-9EEB-75BBE910F48CQ35232180-0E1D1D5B-1010-4D4D-83CF-196B775C00B9Q35232185-D0A025D1-9E4C-406F-B1A2-477E12CF0E4DQ35570167-7CD6C37F-CF7F-46B9-9E64-313B22B3E86CQ35570250-008C4672-502E-4F3D-B434-655CF060DFF1Q35570813-1B2A6D7C-4E20-4EBE-9B43-E924DED4A776Q35570883-2AB846F0-4BBF-434A-931F-2E9821BAAF6B
P2860
Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome.
description
1968 nî lūn-bûn
@nan
1968 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1968 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1968年の論文
@ja
1968年論文
@yue
1968年論文
@zh-hant
1968年論文
@zh-hk
1968年論文
@zh-mo
1968年論文
@zh-tw
1968年论文
@wuu
name
Autosomal trisomy syndromes: a ...... 27 cases of Patau's syndrome.
@ast
Autosomal trisomy syndromes: a ...... 27 cases of Patau's syndrome.
@en
Autosomal trisomy syndromes: a ...... 27 cases of Patau's syndrome.
@nl
type
label
Autosomal trisomy syndromes: a ...... 27 cases of Patau's syndrome.
@ast
Autosomal trisomy syndromes: a ...... 27 cases of Patau's syndrome.
@en
Autosomal trisomy syndromes: a ...... 27 cases of Patau's syndrome.
@nl
prefLabel
Autosomal trisomy syndromes: a ...... 27 cases of Patau's syndrome.
@ast
Autosomal trisomy syndromes: a ...... 27 cases of Patau's syndrome.
@en
Autosomal trisomy syndromes: a ...... 27 cases of Patau's syndrome.
@nl
P2860
P1476
Autosomal trisomy syndromes: a ...... 27 cases of Patau's syndrome.
@en
P2093
P2860
P304
P407
P577
1968-09-01T00:00:00Z