| 000 | 01544 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250511130818.0 | ||
| 264 | 0 | _c19790313 | |
| 008 | 197903s 0 0 eng d | ||
| 022 | _a0340-6717 | ||
| 024 | 7 |
_a10.1007/BF00394291 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aNiebuhr, E | |
| 245 | 0 | 0 |
_aThe Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features. _h[electronic resource] |
| 260 |
_bHuman genetics _cNov 1978 |
||
| 300 |
_a227-75 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Review | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aBirth Order |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 | _aChromosomes, Human, 4-5 |
| 650 | 0 | 4 |
_aCri-du-Chat Syndrome _xdiagnosis |
| 650 | 0 | 4 |
_aCrying _xphysiology |
| 650 | 0 | 4 | _aDermatoglyphics |
| 650 | 0 | 4 |
_aDystonia _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGenitalia _xabnormalities |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aKaryotyping |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMaternal Age |
| 650 | 0 | 4 |
_aMicrocephaly _xgenetics |
| 650 | 0 | 4 |
_aMicrognathism _xgenetics |
| 650 | 0 | 4 | _aPaternal Age |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPrenatal Diagnosis |
| 650 | 0 | 4 | _aSex Ratio |
| 650 | 0 | 4 | _aTranslocation, Genetic |
| 773 | 0 |
_tHuman genetics _gvol. 44 _gno. 3 _gp. 227-75 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/BF00394291 _zAvailable from publisher's website |
| 999 |
_c387711 _d387711 |
||